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International Conference on Marketing, Tourism & Hospitality (gvc)

International Conference on Marketing, Tourism & Hospitality

 

Dear & Esteemed Colleagues,

On behalf of the conference advisory board, it is our pleasure to extend a warm welcome to you to be part of the upcoming International Conference on Marketing, Tourism and Hospitality being jointly organized by Global Business Research Journals (GBRJ) & Greater Vision happening in the beautiful and vibrant city of Bangkok, Thailand.

Kindly submit your abstracts/ full papers/ posters/ case studies in all areas of marketing, tourism and hospitality You may also submit your abstracts/full papers/case studies using the ‘online submission window’ available at the ‘paper submission’ page.

In addition, one of the interesting features and attractions of our conferences is that, in addition to paper presentations, we do organize a panel discussions/invited lectures for the benefit of the global academic community. In Bangkok, the Panel Discussion topic will be, “Integrating Technology into Teaching”. We are, pretty sure that this discussion would add greater value to enhance your support to your students.

Important Dates!

Abstract or Full Paper or Case Studies or Posters Submission Deadline : November 20, 2020
Communication of Acceptance : Three Days
Last Date for Registration : December 20, 2020
Conference Dates : February 15-16, 2020


Conference Objectives!

Tourism, as you would concur, is a great revenue generator and also it bring a lot of social, economic, cultural benefits. In a few countries, tourism is the main driver of economic growth and socio-economic development. It is, indeed, a pleasant privilege to host this upcoming conference in the vibrant city of Bangkok, Thailand, which is considered to be one of the fabulous tourism destinations in the world.

Tourism creates a lot of job opportunities for the citizens and brings social, economic, cultural and other benefits. In many countries, tourism is the main driver of growth and development. Of course, it is, indeed, very appropriate to hold a conference in the beautiful city of Bangkok-Thailand, which is one of the major tourist destinations for many nationalities. The government of Thailand, quite obviously, gives a lot of emphasis on tourism, more particularly, for eco-tourism.
Eco-tourism! An Emerging Paradigm!

Ecotourism is now defined as "responsible travel to natural areas that conserves the environment, sustains the well-being of the local people, and involves interpretation and education" (TIES, 2020). Education is meant to be inclusive of both staff and guests.
Principles of Ecotourism

Ecotourism is about uniting conservation, communities, and sustainable travel. This means that those who implement, participate in and market ecotourism activities should adopt the following ecotourism principles:

Minimize physical, social, behavioral, and psychological impacts, build environmental and cultural awareness and respect, provide positive experiences for both visitors and hosts, provide direct financial benefits for conservation, generate financial benefits for both local people and private industry, deliver memorable interpretative experiences to visitors that help raise sensitivity to host countries' political, environmental, and social climates, design, construct and operate low-impact facilities, recognize the rights and spiritual beliefs of the Indigenous People in your community and work in partnership with them to create empowerment. (Source: http://www.ecotourism.org/what-is-ecotourism)

Against this background, the International Academic Research Conference on Marketing & Tourism is being jointly organized by Greater Vision Conferences & Seminars & the Global Business Research Journals (GBRJ) for two days, February 15-16, 2020.

You are cordially invited to submit your research papers and share your findings before the global audience. We have also made arrangements for a few invited

We earnestly believe that the upcoming conference will be very helpful to share the best practices with the global audience.

Publication Opportunities: Delegates attending our conferences have an opportunity to get their research papers published after following the double-blind review process. On an average, it takes about 60 days to get your papers published in our journals after the conference provided you clearly improve your paper as per the comments and feedback given by the reviewers.

 

ICT19Thailand Conference
Program Outline

Friday, February 15, 2020
Timeline Description of Events
08.30 - 09.30 Registration
09.30 - 10.30 Inaugural Session/Keynote address
10.30 - 11.00 Coffee Break
11.00 - 12.45 Technical sessions - Paper Presentations
12.45 - 14.00 Lunch Break & Networking
14.00 - 14.30 Panel Discussion
14.30 - 15.45 Technical Sessions – Paper Presentations
15.45 - 16.00 Coffee Break
16.00 - 18.00 Technical sessions – Paper Presentations


Presentation Room Meeting Room
Saturday, February 16, 2020
Timeline Description of Events
09.00 - 10.30 Technical sessions – Paper Presentations
10.30 - 11.00 Coffee Break
11.00 - 11.30 Invited Lecture Sessions – All Delegates
11.30 - 12.45 Technical Sessions – Paper Presentations
12.45 - 14.00 Lunch Break
14.00 - 15.00 Invited Lecture Session – All Delegates
15.00 - 15.30 Coffee break
15.30 – 17.00 Technical Sessions– Paper Presentations
Presentation Room Meeting Room


Scientific Advisory & Review Board.
Dr. Andrew Papadimos, Australian Catholic University, Australia.
Dr. Cenap Ilter, California State University Dominguez Hills, USA.
Dr. K.H. LEE, TBSS Center for Electrical and Electronics Engineering, Singapore.
Dr. Leng Ho Keat, Nanyang Technological University, Singapore.
Dr. M. Mert ASLAN, Selcuk University, Turkey.
Dr. Min-Teh Yu, China University of Technology, Taiwan.
Dr. Nguyen Anh Phong, University of Economics and Law, Vietnam.
Dr. R. Rajasekaran, PSG College of Arts and Science, India.
Dr. Wai Chung Yeong, Universiti Malaya, Malaysia.
Dr. Xuan Duong Nguyen, Hong Duc University, Vietnam.
Dr. Yong Kyu Lew, Hankuk University of Foreign Studies, Korea (South).
Dr. Yoshimasa (Nancy), Kageyama, Missouri State University, USA.
Prof. Abu N.M. Wahid, Tennessee State University, USA.
Prof. Byungchul Choi, Hankuk University of Foreign Studies, Korea (South).
Prof. Dr. Hatane Semuel, Petra Christian University, Indonesia.
Prof. Jaypy T. Tenerife, Technological Institute of the Philippines, Philippines.
Prof. Joefrelin C. Ines, Shinas College of Technology, Oman.
Prof. Joonil KIM, Mokwon University, Korea (South).
Prof. Marilou Q. Tolentino, Systems Plus College Foundation, Philippines.

 

Please contact the event manager Marilyn ([email protected] ) below for:
- Multiple participant discounts
- Price quotations or visa invitation letters
- Payment by alternate channels (PayPal, check, Western Union, wire transfers etc)
- Event sponsorships

NO REFUNDS ALLOWED ON REGISTRATIONS
Service fees included in this listing.
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9th International Conference on Pharmaceutical GMP, GCP & Regulatory Affai...

9th International Conference on Pharmaceutical GMP, GCP & Regulatory Affairs

About

2020 Key ThemesRegulatory Affairs 2020 conference will focus on new strategies, amendments, innovations, developments in the fields of regulatory affairs, intellectual property rights and medical devices with the theme: “Current challenges of Pharmaceutical & Biopharmaceutical Industries in regulatory framework” which reflects new strategies in the field of regulatory affairs. This conference includes workshops, symposiums, special sessions, key note sessions, conducted by eminent and renowned speakers who excel in the field of regulatory affairs, medical devices, intellectual property rights which include the topics regulatory affairs in pharmacovigilance, clinical affairs & regulatory strategies, regulatory strategies and developments, penalties of regulatory Non-compliance, biologics & biosimilars, global regulatory intelligence, Impact of Brexit on regulatory framework, regulatory requirements in pharmaceuticals, regulatory challenges for medical devices, medical device and combination products regulation, Intellectual property rights etc. This International Regulatory Affairs Conference also encourages the active participation of Young Researchers, Students as we are hosting Poster Award Competition and Young Research Forum at the conference venue.

Product Registration & Submission
Global Guidelines for the Development of Biologics
Medical Device & Combination Products Regulations
Accelerating Approval of New Drugs
ASEAN Labelling Harmonisation
Regulatory & Clinical Affairs
Regulatory & Pharmacovigilance
Regulatory Enforcement & Inspection

Target Audience:

Regulatory Affairs experts
Clinical Research Associates
Medical Devices experts
Quality Assurance experts
Intellectual Property Rights attorneys
Scientists
Researchers
Academicians
Industrialists

Continent wise participation Analysis for Regulatory Affairs 2020 conference

Session/Tracks

Track 1: Regulatory Affairs

Regulatory Affairs profession was developed by the government regulatory bodies to regulate the safety and efficacy of products to protect the health of public. This was developed in all most all divisions of health care industry like pharmaceuticals, veterinary medicines, medical devices, pesticides, agrochemicals, cosmetics, complimentary medicines etc. This profession involves development of new and existing products from early on, preparation and till submission to the relevant regulatory bodies of health authorities by inputting regulatory principles.

Regulatory Affairs is involved actively from early stage of development to post marketing activities of new and existing products. This department is one of the integral parts within the organization structure of pharmaceutical industry. Internally it collaborates at the interphase of drug development, manufacturing, marketing and clinical research. Externally it is the key interface between the commercial industry which undergoes drug development to clinical research and the regulatory authorities.

Track 2: Regulatory Affairs in Pharmacovigilance

Regulatory Affairs (RA), likewise called government issues, are a calling inside managed enterprises, for example, pharmaceuticals, medicinal gadgets, vitality, saving money, telecom and so on. Administrative Affairs likewise has a certain importance inside the human services enterprises (pharmaceuticals, therapeutic gadgets, biologics and useful nourishments). Administrative issues (therapeutic issues) experts (otherwise known as administrative experts) typically have duty regarding the accompanying general territories.

Pharmacovigilance evaluates the adverse effects in turn speaking about the efficacy and safety data of particular drug product thus, collaboration of pharmacovigilance with regulatory bodies provides all the adverse reactions, safety data to regulatory authorities.

Working with government, state and neighborhood administrative offices and faculty on particular issues influencing their business i.e., working with so much office as the Food and Drug Administration or European Medicines Agency (pharmaceuticals and restorative gadgets); The Department of Energy; or the Securities and Exchange Commission (banking). Advising their organizations on the administrative angles and atmosphere that would influence proposed exercises. i.e., portraying the "administrative atmosphere" around issues, for example, the advancement of professionally prescribed medications and Sarbanes-Oxley consistence.

Track 3: Clinical Affairs & Regulatory Strategies

An administrative science driven administrative procedure is crucial as a component of today's biopharmaceutical item early advancement arranging. An all-around arranged administrative methodology will adjust the proposed clinical advancement arrangement with business targets, and pre-emptively distinguish challenges, and also, proposed elective/creative ways to deal with new item improvement which influence new measures for confirmation era supporting proceeding with improvement and worldwide business sector approval. An administrative methodology characterizes key issues/difficulties to proactively talk about with Regulatory powers furthermore characterizes key system points of reference that are frequently considered business impetuses driving speculator intrigue and financing. In particular, an auspicious, very much arranged and all around kept up administrative technique, with proactive and collective cooperation with administrative powers, is regularly a separating element for industry pioneers putting up monetarily fruitful and creative items for sale to the public in today's aggressive commercial center. Administrative procedure is a noteworthy segment of fruitful biopharmaceutical item improvement. Covance Global Regulatory Affairs gets ready and keeps up administrative science driven and item particular worldwide administrative systems for some item sorts, e.g., drugs, biologics, drug-gadget mixes, antibodies, quality treatments, cell-treatments, over a scope of restorative territories and full administrative technique support for item improvement activities.

Track 4: Regulatory Strategies and Developments

Regulatory strategies are formal documents that include series of regulatory activities to discover an innovative product or a modified product to market with business strategy for that product. This provides description and course to project team for the product being developed with identification of important regulatory elements which are addressed to market the product. Within a firm there are many regulatory strategists from different departments that involve all aspects of a drug and individuals with expertise in chemical synthesis, toxicology, biology, clinical and regulatory affairs, marketing, government affairs and reimbursement inputs into the regulatory strategy ensuring it is comprehensive.

Regulatory strategy document has three purposes, it acts as a:

A tracking tool to summarize key agreements reached with health authorities
A planning tool that documents timelines and lists topics to address in future meetings with health authorities
A risk register to record key issues that could impact timelines, costs or commercial value for the project

Track 5: Penalties for Regulatory Non-compliance:

Non-compliance costs are costs which result from a failure to comply with regulation. These costs are not considered to be part of the regulatory burden for the purposes of the Risk Based Monitoring. This includes penalties and activities associated with those penalties that are required to be undertaken because of noncompliance with regulation. Regulatory impacts that arise, up to the point that action is taken to respond to the suspicion of a specific instance of noncompliance, are included in RBM framework. This includes risk based frameworks that may target certain populations without a specific instance of suspicion. Failure to comply with the law can lead to enforcement action including one or more of the following: on-the-spot fines, prosecution, which carries a maximum fine of $12,110, disciplinary action, ranging from fines to cancellation of the license.

Track 6: Biologics & Biosimilars

A biopharmaceutical, otherwise called a biologic therapeutic item or biologic, is any restorative item made in, extricated from, or semi orchestrated from organic sources. Not quite the same as synthetically incorporated pharmaceuticals, they incorporate immunizations, blood, or blood segments, allergenic, substantial cells, quality treatments, tissues, recombinant restorative protein, and living cells utilized as a part of cell treatment. Biologics can be made out of sugars, proteins, or nucleic acids or complex mixes of these substances, or might live cells or tissues. They are confined from normal sources—human, creature, or microorganism. Phrasing encompassing biopharmaceuticals fluctuates amongst gatherings and elements, with various terms alluding to various subsets of therapeutics inside the general biopharmaceutical class. Some administrative offices utilize the terms natural restorative items or remedial organic item to allude particularly to designed macromolecular items like protein-and nucleic acid–based drugs, recognizing them from items like blood, blood segments, or antibodies, which are typically extricated specifically from a natural source Gene-based and cell biologics, for instance, frequently are at the front line of biomedical research, and might be utilized to treat an assortment of therapeutic conditions for which no different medications are accessible.

Track 7: Global Regulatory Intelligence

Ever-proliferating and changing global regulations generate complex challenges of execution in global market clearance operations.

Mission-critical decisions are delayed, trapping new international revenue until market clearance process issues are resolved. Workflow is confounded as information conflicts from sales-focused distributors, newly-appointed foreign regulators, and legacy resources are reconciled- and as definitive answers are sought. Governance is compromised as information gaps reduce assurance levels and impair risk management of clearance-related penalties, fines, and legal costs.

And the high level of business performance required to create value from ongoing medtech industry consolidation is not achievable, since global market clearance operations are incapable of rapidly completing new market clearance submissions for newly-acquired product lines.

Unlike repackaged RI databases designed for the pharmaceutical industry, the clinivation Worldview Enterprise Solution for On-Demand Global Regulatory Intelligence accelerates the market clearance cycle.

Track 8: Impact of Brexit on Regulatory Framework

The most important piece of UK legislation that would need to be repealed is the European Communities Act 1972 (ECA), which provides for the supremacy of EU law. Repealing the ECA will bring an end to the constitutional relationship that exists between EU and UK law. Moreover, the vast amounts of secondary legislation that have been passed with the objective and justification of implementing EU law would have to be considered by the Government. EU Regulations rely on the principle of direct applicability, which means that unlike EU Directives, they are directly implemented into UK law without the need for legislation from the UK Parliament. In this light, Regulations are more powerful legislative tools for the EU because of their immediate applicability. The status of existing Regulations will be addressed in the Great Repeal Bill, although as noted above, in many cases amendments will likely be needed to take into account the UK’s new relationship with the EU. The Court of Justice of the European Union (CJEU) situated in Luxembourg is the final arbiter on questions of the interpretation of EU law. In her first speech setting out the UK Government’s priorities for Brexit on 17 January 2020, the Prime Minister restated her position that the UK is not prepared to continue to be subject to the jurisdiction of the CJEU.

Track 9: Regulatory Communications and Submissions

Due to the growing interest in marketing new products, it is pivotal to establish a superior level of medical writing and regulatory operations. Executives within these roles need to create and manage successful submissions, as well as streamline timelines, to accelerate approval.

Attending the Optimizing Regulatory Communications and Submissions conference will aid delegates in expediting the approval of drugs while meeting requirements for different regulatory agencies worldwide. In addition, attendees will overcome key operational challenges impacting the approval process to enhance the quality of submissions.

Track 10: Marketing Authorizations-Affordable Healthcare and Fair Trade

This establishment level module is the perfect acquaintance for new participants with the field of pharmaceutical administrative issues and consistence. It portrays the central prerequisites that must be fulfilled to pick up and keep up endorsement to advertise restorative items in the USA and Europe. The lawful structure and the parts of significant players in control are displayed. The life-cycle of a medication is sketched out. The different systems accessible for appraisal and endorsement of items are depicted and their prerequisites laid out. Commitments to be satisfied in the wake of promoting endorsement are examined. Worldwide administrative undertakings bunches in industry give around the world, key initiative in and far reaching course of the legislature administrative necessities for item presentation and commercialization, using administrative learning to guarantee consistence and administrative knowledge and make open doors in an exceedingly controlled environment. The worldwide administrative undertakings bunch has vital and operational capacities, requiring accuracy and faultless execution, as an organization's prosperity depends on, partially, the direction and thorough appraisal gave by the administrative issues group. The key item advancement, assembling and enlistment turning points, (for example, Investigational New Drug documenting, end of stage II, stage III, New Drug Application entries, administrative office audit timetable and item endorsements), which are the corporate valuation and choice focuses, depend on basic administrative interface goalposts and developments. This underscores the significance of key administrative commitment to the business. Keeping in mind the end goal to be profitable donors and basic business accomplices, the worldwide administrative undertakings association must create instruments and build up frameworks to guarantee it has the right individuals and ability, capable procedures, productive profitability, sensational execution and accuracy in arranging.

Track 11: Regulatory Requirements for Pharmaceuticals

The new medication endorsement process have been made into three stages for improvement in comprehension - the principal stage is pre-advertising implied for revelation, advancement and clinical concentrates, second stage for promoting approval of medication and third is for post showcasing. Firstly, preclinical investigations of a medication are finished to guarantee adequacy and security, and after that application for behavior of clinical trials is submitted to the CDSCO. From that point, the clinical trials can be led (stage I to stage IV). These studies are performed to guarantee the viability, wellbeing and upgrading the measurements of medication in people. After the culmination of clinical investigations of the medication, then an application to the skilled power of India for the endorsement of medication for advertising is submitted. The able power audit the application and affirm the medication for advertising just if the medication is observed to be sheltered and successful in individual or the medication have more alluring impact as contrast with the danger.

Track 12: Regulatory Challenges for Medical Devices

As therapeutic gadget quality certification and administrative undertakings experts, it can test to remain focused of changes occurrence in our industry. Administrative controls for restorative gadgets are rare in the creating scene, despite the fact that usage of national medicinal gadget directions will frequently address the very issues brought up in nations as significant attentiveness toward patient wellbeing. Case of these issues incorporate the unlawful re-preparing and re-bundling of utilized syringes for re-deal; the accessibility available of hardware that fizzles least quality and security benchmarks; or just no hint of what gadgets are being sold in the nation, nor by whom. Such a posting is crucial to empower governments to issue cautions or reviews for perilous or inadequate things.

Track 13: Medical Device & Combination Products Regulations

Blend items are remedial and indicative items that consolidate medications, gadgets, and/or organic items. FDA hopes to get expansive quantities of blend items for audit as innovative advances keep on merging item sorts and obscure the verifiable lines of partition between FDA's therapeutic item focuses, which are comprised of the Center for Biologics Evaluation and Research (CBER), the Center for Drug Evaluation and Research (CDER), and the Center for Devices and Radiological Health (CDRH). Since mix items include parts that would regularly be controlled under various sorts of administrative powers, and much of the time by various FDA Centers, they raise testing administrative, strategy, and audit administration challenges. Contrasts in administrative pathways for every part can affect the administrative procedures for all parts of item improvement and administration, including preclinical testing, clinical examination, showcasing applications, assembling and quality control, antagonistic occasion reporting, advancement and promoting, and post-endorsement alterations.

Track 14: Best Industry Practices

Drug business is one in everything about nation's most critical monetary motors, trade $15 billion in stock yearly and a couple of its processing plants region unit preeminent. The government office has built up a progression of tips for creating GXP (which incorporates GCP, GLP and GMP directions) that shield each the life sciences business furthermore the clients they serve. In order to help FDA-directed firms, expert control offers partner in incorporated quality and consistence administration code that guarantees GLP, GCP and GMP rules consistence. Industry practices is likewise some portion of value danger administration framework, Pharma Regulatory Affairs, Audits and assessments, acceptance strategies (process approval and expository approval), Qualification, acceptance, adjustment, upkeep, hazard investigation Drug Safety and Good Pharmacovigilance hones. Some of our product framework applications which will encourage with GLP GCP GMP rules epitomize the resulting arrangements: Document Control/Document Management, Corrective Action Preventive Action (CAPA), alteration administration, guiding Management, resistance Automation programming framework, Audit Management in venture with GLP GCP GMP rules, customer protests programming framework, shapes based strategy robotization, electronic entries.

Track 15: Intellectual Property Rights

In the EU, an organic thoughtful item is one amongst the dynamic substance(s) made from or separated from a natural (living) framework, and requirements, also to physico-compound testing, natural testing for full characterization. The characterization of a natural medicative item could be a blend of testing the dynamic substance and hence the last medicative item along the edge of the get together strategy and its administration. Central thoughts of Intellectual Property Management (IPM) and its significance is a goad to human force and in this manner is the headway of financial and social improvement. It furthermore gives defense on the occasion Associate in usage of an IPM technique together with the administration of material ownership (IP) in a web setting. Investigative control law more often than not gives the creator of partner in scholarly creation restrictive rights for abusing and taking advantage of their creation. Experimental order insurance is intended to fortify the force of the human personality for the upside of all by verifying that benefits got from misusing a creation advantage the maker. This may energize action and allow financial specialists in investigation and improvement a decent go ahead their speculation. Experimental order presents on individuals, undertakings or option elements the right to bar others from the vocation of their manifestations wellbeing and quality control in naming. Therefore, material ownership rights (IPRs) could have an on the spot Associate in generous effect on exchange on the grounds that the proprietor of an IPR could - through the social control of such a privilege - prevent the assembling, use or offer of an item which incorporates the IPR. Therefore administration over the immaterial (IPR) suggests administration of the stock and markets. Exploratory order security energizes the production, conveyance and discourse demonstration of the creation to the overall population, rather than keeping it mystery though at indistinguishable time urging mechanical endeavours to choose imaginative works for abuse. Material ownership lawful titles identifies with the securing and utilization of an assortment of rights covering totally distinctive type of manifestations. Licenses in the pharmaceutical business incorporate both lawful and moral issues.

Please contact the event manager Marilyn (marilyn.b.turner(at)nyeventslist.com ) below for:
- Multiple participant discounts
- Price quotations or visa invitation letters
- Payment by alternate channels (PayPal, check, Western Union, wire transfers etc)
- Event sponsorship

NO REFUNDS ALLOWED ON REGISTRATIONS
Prices may go up any time. Service fees included in pricing.
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Conference on Pharmaceutical Analysis & Analytical Chemistry (cse) AS

2nd International Conference on Pharmaceutical Analysis & Analytical Chemistry

 


Pharmaceutical Analysis 2020

 

After the fruitful execution of the International Conference on Pharmaceutical Analysis and Quality Control Strategies, Conference Series with great pride and honour announcing its International Conference on Pharmaceutical Analysis & Analytical Chemistry which is going to held in Chicago, USA during August 02-03, 2020.

Pharmaceutical Analysis 2020 serves as a podium for the interaction between experts in the area of pharmaceutical analysis and analytical chemistry around the world. We cordially invite all the eminent researchers, academicians, students, industry representatives working in these exciting areas.

This Conference is mainly focused on the theme “New paradigms in Pharmaceutical Analytical Techniques”. The conference includes workshops, symposiums, special keynote sessions conducted by eminent and renowned speakers who excel in the field of Pharmaceutical Analysis and Drug Discovery This International Pediatric Conference also encourages the active participation of young student researchers as we are hosting Poster Award Competition and Young research Forum at the conference venue.

Target Audience:

  • Pharmaceutical Analysis Researchers

  • Analytical Chemists

  • Noble Laureates

  • Directors, Presidents, CEO’s of Organizations/Companies

  • Pharmaceutical Associations and Societies

  • Academicians (Professors, Associate & Assistant professors, Deans, Directors)

  • Graduates and Post graduates

 

Sessions/Tracks

Track 1: Modern Pharmaceutical Analysis

Generally, Pharmaceutical Analysis alluded to the synthetic examination of medication atoms. Be that as it may, throughout the years, present day pharmaceutical investigation has advanced past this to envelop mix systems, high-throughput innovations, chemo metrics, micro dosing studies, scaling down and nanotechnology. These logical advances are currently being utilized in all phases of medication disclosure and the concentration of this survey will be on how these advances are being utilized inside this procedure. With new, enhanced and advancing innovations, and in addition new applications for existing innovation, the scan for new medications for the aversion and treatment of human maladies proceeds.

 

Track 2: Chromatography & Separation Techniques

Chromatography strategy for isolating the parts, or solutes, of a blend on the premise of the relative measures of every solute appropriated between a moving liquid streams, called the versatile stage, and a touching stationary stage. The versatile stage might be either a fluid or a gas, while the stationary stage is either a strong or a liquid. Increase in advances in Biotechnology sector augments the production of variety of valuable bio products. Molecules such as therapeutic proteins, enzymes, and other important products require combination of chromatography so as to purify them in purest form. Combination of these novel technologies minimizing the purification steps plays a crucial role for getting maximum purification of the biomolecules.

 

Track 3: Analytical Method Development and Validation

Analytic method development and validation are persistent and interconnected exercises directed all through the drug development process. The act of validation checks that a given method measures a parameter as planned and sets up the execution furthest reaches of the estimation. Albeit clearly conflicting, approved methods create comes about inside known vulnerabilities. These outcomes are essential to proceeding with drug development, as they characterize the rising learning base supporting the product. The time and exertion that are put into growing logically solid, hearty, and transferrable analytic methods ought to be lined up with the drug development arrange. The assets that are consumed on method validation must be constantly balanced with regulatory requirements and the likelihood for product commercialization.

 

Track 4: Spectroscopy and its Techniques

Spectroscopy deals with surplus of different techniques that employ electromagnetic radiation on materials in order to measure and interpret data, which is used for elucidating a variety of analytical problems. It includes absorption, emission, or scattering of electromagnetic radiation by atoms or molecules. Types of spectroscopy are IR & NIR, UV/visible, NMR, Atomic Emission Spectroscopy, Fluorescence Spectroscopy etc. Spectroscopic methods are used for Environmental Analysis, Biomedical studies, astronomy. UV-Visible Spectrometer is used for a varied range of applications.

 

Track 5: Pharmaceutical and Biomedical Analysis

Analytical biochemistry is the study of biochemical components found in a cell or other biological sample. This field uses a broad vary of techniques for separation, identification, quantification and practical characterization of biological molecules like nucleic acids, enzymes, proteins, pigments, carbohydrates and additional. The main ways involved in analytical biochemistry to separate the biological components are qualitative analysis techniques, chromate graphical Techniques, super molecule Estimation & Purification Techniques and medicine Techniques.

 

Track 6: Mass Spectroscopy: Approaches and Challenges

New mass spectrometry (MS) methods, collectively known as data independent analysis and hyper reaction monitoring. Last decade has witnessed remarkable technological advances in mass spectrometry based proteomics and Biologics. Specific advances include high throughput protein identification by multidimensional chromatography, automated tandem mass spectrometry and sequence data base searching, accurate quantification by the application of stable isotope dilution theory to protein analysis, and the targeted isolation of selected analytes by the use of highly selective chemistries.

 

Track 7: Bioanalysis

Bioanalysis involves the quantitative measurement of xenobiotics (drugs and their metabolites, and biological molecules in unnatural locations or concentrations) and biotics (macromolecules, proteins, DNA, large molecule drugs, metabolites) in biological systems. In the past two decades, has seen increase in the field of Biopharmaceuticals. Bioanalysis applies to the drugs used for anti-doping testing in sports, illicit purposes and Environmental concerns. The most frequently used techniques are liquid chromatography coupled with tandem mass spectrometry (LC–MS/MS) for micro molecules and enzyme-linked immunosorbent assay (ELISA) for macromolecules.

 

Track 8: Electro chemical and Thermo analytical techniques

Electrochemical Analysis is a powerful technique that is increasing in utility in the Pharmaceutical Industry due to its high sensitivity, speed of analysis, reduction in solvent and sample consumption, and low operating cost compared to other analytical methods. The modern Electrochemical Analytical techniques are cyclic, linear sweep, differential pulse, square wave and stripping voltammetric techniques. Thermo Analytical techniques are mainly used to detect compound purity, polymorphism, solvation, degradation, and excipient compatibility. It is extensively used in conducting Preformulation studies.

 

Track 9: Analytical Chemistry

Analytical Chemistry has many applications in Forensic Sciences, environmental analysis, and materials analysis. Analytical Chemistry research is mainly driven by the performance and cost. In these days, great efforts are being put to shrinken the analytical techniques to chip size. In this technology, the most used technique is lab-on-a-chip. The ongoing developments of computer automation and information technologies have broadened the analytical chemistry into a number of new biological fields.

 

Track 10: Preformulation Studies

Preformulation is considered as critical decision-making tool during both – drug discovery and development phase. Preformulation studies help in assessing the drugability of a molecule. To generate Preformulation data analytical techniques like Spectroscopic, Chromatographic, Thermal methods and some specific detection methods like Capillary electrophoresis are used.

 

Track 11: Hyphenated Techniques in Analytical chemistry

Hyphenated technique is developed from the coupling of a separation technique and an on-line spectroscopic detection technology. These techniques are mainly broadened their applications in the analysis of natural products.

 

Track 12: Quality Assurance and Quality Control

Quality assurance is defined as a procedure or set of procedures intended to ensure that a product or service under development meets specified requirements. Quality control (QC) is a procedure or set of procedures intended to ensure that a manufactured product or performed service adheres to a defined set of quality criteria that meets the requirements of the client or customer. The two approaches can be thought of simply as failure detection (QC) and failure prevention (QA). The ISO 9000 family of quality management systems standards is designed to help organizations ensure that they meet the needs of customers and other stakeholders while meeting statutory and regulatory requirements related to a product or service.

 

Track 13: Pharmaceutical Analysis Errors and Validation

Analytical errors are fundamental before submitting your report and results with the required level of confidence. However, we should have clarity regarding accuracy and precision before we are talking pharmaceutical error. Most of us believe that these terms have the same meaning but the example of arrows striking a target. Any measurement is limited by the precision of the measuring instruments and the technique and the skill of the observer. Where a measurement consists of a single reading on a simple piece of laboratory equipment, for example, a burette or a thermometer, one would expect the quantity of factors adding to vulnerabilities in that estimation to be less than an estimation which is the consequence of a multi-step process comprising of at least two weight estimations, a titration and the utilization of an variety of reagents.

 

Track 14: GLP and GMP Method Development, Validation and Remediation

Good manufacturing practice is the piece of quality assurance which ensures that things are reliably made and controlled to the quality standard proper to their proposed use and as required by the Marketing Authorization or item particular. GMP is stressed over both generation and quality control, consistency with this standard gives open assurance that the rights, security, and prosperity of trial subjects are ensured; predictable with the rule that have their starting point in the Declaration of Helsinki, and that the clinical information is valid.

 

Track 15: Biosensors

Biosensor is a device which converts the information regarding the presence of a compound into electro analytical Signal. The biosensor research areas include modern Bio specific analytical techniques. In the recent years, micro fabrication techniques have showed a significant improvement in biosensor systems. The modern methods of the biosensor discoveries range from electrochemical, electromechanical, and fluorescence-­cum-optical-based biosensors and genetically engineered microbes.

 

Track 16: Pharmaceutical Microbiology

Modern microbiology is unmistakably a branch of biotechnology and incorporates the customary and nucleic corrosive aspects. Pharmaceutical microbiology is the connected branch of microbiology which enables drug specialists to make pharmaceuticals from microorganisms either straightforwardly or with the utilization of some item delivered by them. Different parts of pharmaceutical microbiology incorporate innovative work for assembling of different hostile to tumours, against microbial specialists.

 

Track 17: Forensic Analysis

Multiply hyphenated techniques, such as gas chromatography/ mass spectrometry with retention time locking (GC/MS/RTL), liquid chromatography/time-of-flight mass spectrometry (LC/ MS/TOF), micro fluidic-based capillary electrophoretic analysis of mitochondrial DNA (mtDNA), and laser ablation inductively coupled plasma mass spectrometry (LA/ICP/MS), are able to uncover forensically germane information by providing unprecedented levels of analytical selectivity and sensitivity

 

Track 18: Radio Analytical Techniques

Radio analytical Techniques focuses on analysis of sample for their radionuclide content. The Radio analytical Chemistry Capability (RACC) combines radioanalytical chemistry and medium level gamma-ray spectrometry. It has wide applications in the field of forensics, atmospheric sciences, health protection, archeology, and engineering

 

Why to Attend

Pharmaceutical Analysis will provide you a great opportunity to meet with like-minded people and industry peers. This is the best place to present your research in front of the global audience coming from the different countries. World-renowned speakers, the most recent techniques, developments, and the newest updates in Pharmaceutical Analysis are the hallmarks of this conference.

 

Please contact the event manager Marilyn ([email protected] ) below for:
- Multiple participant discounts
- Price quotations or visa invitation letters
- Payment by alternate channels (PayPal, check, Western Union, wire transfers etc)
- Event sponsorships

NO REFUNDS ALLOWED ON REGISTRATIONS
Service fees included in this listing.
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2nd International Conference on Pharmaceutical Analysis & Analytical Chemi...

2nd International Conference on Pharmaceutical Analysis & Analytical Chemistry

About

After the fruitful execution of the International Conference on Pharmaceutical Analysis and Quality Control Strategies, Conference Series with great pride and honour announcing its International Conference on Pharmaceutical Analysis & Analytical Chemistry which is going to held in Chicago, USA during August 02-03, 2020.

Pharmaceutical Analysis 2020 serves as a podium for the interaction between experts in the area of pharmaceutical analysis and analytical chemistry around the world. We cordially invite all the eminent researchers, academicians, students, industry representatives working in these exciting areas.

This Conference is mainly focused on the theme “New paradigms in Pharmaceutical Analytical Techniques”. The conference includes workshops, symposiums, special keynote sessions conducted by eminent and renowned speakers who excel in the field of Pharmaceutical Analysis and Drug Discovery This International Pediatric Conference also encourages the active participation of young student researchers as we are hosting Poster Award Competition and Young research Forum at the conference venue.

Target Audience:

Pharmaceutical Analysis Researchers

Analytical Chemists

Noble Laureates

Directors, Presidents, CEO’s of Organizations/Companies

Pharmaceutical Associations and Societies

Academicians (Professors, Associate & Assistant professors, Deans, Directors)

Graduates and Post graduates

Sessions/Tracks

Track 1: Modern Pharmaceutical Analysis

Generally, Pharmaceutical Analysis alluded to the synthetic examination of medication atoms. Be that as it may, throughout the years, present day pharmaceutical investigation has advanced past this to envelop mix systems, high-throughput innovations, chemo metrics, micro dosing studies, scaling down and nanotechnology. These logical advances are currently being utilized in all phases of medication disclosure and the concentration of this survey will be on how these advances are being utilized inside this procedure. With new, enhanced and advancing innovations, and in addition new applications for existing innovation, the scan for new medications for the aversion and treatment of human maladies proceeds.

Track 2: Chromatography & Separation Techniques

Chromatography strategy for isolating the parts, or solutes, of a blend on the premise of the relative measures of every solute appropriated between a moving liquid streams, called the versatile stage, and a touching stationary stage. The versatile stage might be either a fluid or a gas, while the stationary stage is either a strong or a liquid. Increase in advances in Biotechnology sector augments the production of variety of valuable bio products. Molecules such as therapeutic proteins, enzymes, and other important products require combination of chromatography so as to purify them in purest form. Combination of these novel technologies minimizing the purification steps plays a crucial role for getting maximum purification of the biomolecules.

Track 3: Analytical Method Development and Validation

Analytic method development and validation are persistent and interconnected exercises directed all through the drug development process. The act of validation checks that a given method measures a parameter as planned and sets up the execution furthest reaches of the estimation. Albeit clearly conflicting, approved methods create comes about inside known vulnerabilities. These outcomes are essential to proceeding with drug development, as they characterize the rising learning base supporting the product. The time and exertion that are put into growing logically solid, hearty, and transferrable analytic methods ought to be lined up with the drug development arrange. The assets that are consumed on method validation must be constantly balanced with regulatory requirements and the likelihood for product commercialization.

Track 4: Spectroscopy and its Techniques

Spectroscopy deals with surplus of different techniques that employ electromagnetic radiation on materials in order to measure and interpret data, which is used for elucidating a variety of analytical problems. It includes absorption, emission, or scattering of electromagnetic radiation by atoms or molecules. Types of spectroscopy are IR & NIR, UV/visible, NMR, Atomic Emission Spectroscopy, Fluorescence Spectroscopy etc. Spectroscopic methods are used for Environmental Analysis, Biomedical studies, astronomy. UV-Visible Spectrometer is used for a varied range of applications.

Track 5: Pharmaceutical and Biomedical Analysis

Analytical biochemistry is the study of biochemical components found in a cell or other biological sample. This field uses a broad vary of techniques for separation, identification, quantification and practical characterization of biological molecules like nucleic acids, enzymes, proteins, pigments, carbohydrates and additional. The main ways involved in analytical biochemistry to separate the biological components are qualitative analysis techniques, chromate graphical Techniques, super molecule Estimation & Purification Techniques and medicine Techniques.

Track 6: Mass Spectroscopy: Approaches and Challenges

New mass spectrometry (MS) methods, collectively known as data independent analysis and hyper reaction monitoring. Last decade has witnessed remarkable technological advances in mass spectrometry based proteomics and Biologics. Specific advances include high throughput protein identification by multidimensional chromatography, automated tandem mass spectrometry and sequence data base searching, accurate quantification by the application of stable isotope dilution theory to protein analysis, and the targeted isolation of selected analytes by the use of highly selective chemistries.

Track 7: Bioanalysis

Bioanalysis involves the quantitative measurement of xenobiotics (drugs and their metabolites, and biological molecules in unnatural locations or concentrations) and biotics (macromolecules, proteins, DNA, large molecule drugs, metabolites) in biological systems. In the past two decades, has seen increase in the field of Biopharmaceuticals. Bioanalysis applies to the drugs used for anti-doping testing in sports, illicit purposes and Environmental concerns. The most frequently used techniques are liquid chromatography coupled with tandem mass spectrometry (LC–MS/MS) for micro molecules and enzyme-linked immunosorbent assay (ELISA) for macromolecules.

Track 8: Electro chemical and Thermo analytical techniques

Electrochemical Analysis is a powerful technique that is increasing in utility in the Pharmaceutical Industry due to its high sensitivity, speed of analysis, reduction in solvent and sample consumption, and low operating cost compared to other analytical methods. The modern Electrochemical Analytical techniques are cyclic, linear sweep, differential pulse, square wave and stripping voltammetric techniques. Thermo Analytical techniques are mainly used to detect compound purity, polymorphism, solvation, degradation, and excipient compatibility. It is extensively used in conducting Preformulation studies.

Track 9: Analytical Chemistry

Analytical Chemistry has many applications in Forensic Sciences, environmental analysis, and materials analysis. Analytical Chemistry research is mainly driven by the performance and cost. In these days, great efforts are being put to shrinken the analytical techniques to chip size. In this technology, the most used technique is lab-on-a-chip. The ongoing developments of computer automation and information technologies have broadened the analytical chemistry into a number of new biological fields.

Track 10: Preformulation Studies

Preformulation is considered as critical decision-making tool during both – drug discovery and development phase. Preformulation studies help in assessing the drugability of a molecule. To generate Preformulation data analytical techniques like Spectroscopic, Chromatographic, Thermal methods and some specific detection methods like Capillary electrophoresis are used.

Track 11: Hyphenated Techniques in Analytical chemistry

Hyphenated technique is developed from the coupling of a separation technique and an on-line spectroscopic detection technology. These techniques are mainly broadened their applications in the analysis of natural products.

Track 12: Quality Assurance and Quality Control

Quality assurance is defined as a procedure or set of procedures intended to ensure that a product or service under development meets specified requirements. Quality control (QC) is a procedure or set of procedures intended to ensure that a manufactured product or performed service adheres to a defined set of quality criteria that meets the requirements of the client or customer. The two approaches can be thought of simply as failure detection (QC) and failure prevention (QA). The ISO 9000 family of quality management systems standards is designed to help organizations ensure that they meet the needs of customers and other stakeholders while meeting statutory and regulatory requirements related to a product or service.

Track 13: Pharmaceutical Analysis Errors and Validation

Analytical errors are fundamental before submitting your report and results with the required level of confidence. However, we should have clarity regarding accuracy and precision before we are talking pharmaceutical error. Most of us believe that these terms have the same meaning but the example of arrows striking a target. Any measurement is limited by the precision of the measuring instruments and the technique and the skill of the observer. Where a measurement consists of a single reading on a simple piece of laboratory equipment, for example, a burette or a thermometer, one would expect the quantity of factors adding to vulnerabilities in that estimation to be less than an estimation which is the consequence of a multi-step process comprising of at least two weight estimations, a titration and the utilization of an variety of reagents.

Track 14: GLP and GMP Method Development, Validation and Remediation

Good manufacturing practice is the piece of quality assurance which ensures that things are reliably made and controlled to the quality standard proper to their proposed use and as required by the Marketing Authorization or item particular. GMP is stressed over both generation and quality control, consistency with this standard gives open assurance that the rights, security, and prosperity of trial subjects are ensured; predictable with the rule that have their starting point in the Declaration of Helsinki, and that the clinical information is valid.

Track 15: Biosensors

Biosensor is a device which converts the information regarding the presence of a compound into electro analytical Signal. The biosensor research areas include modern Bio specific analytical techniques. In the recent years, micro fabrication techniques have showed a significant improvement in biosensor systems. The modern methods of the biosensor discoveries range from electrochemical, electromechanical, and fluorescence-­cum-optical-based biosensors and genetically engineered microbes.

Track 16: Pharmaceutical Microbiology

Modern microbiology is unmistakably a branch of biotechnology and incorporates the customary and nucleic corrosive aspects. Pharmaceutical microbiology is the connected branch of microbiology which enables drug specialists to make pharmaceuticals from microorganisms either straightforwardly or with the utilization of some item delivered by them. Different parts of pharmaceutical microbiology incorporate innovative work for assembling of different hostile to tumours, against microbial specialists.

Track 17: Forensic Analysis

Multiply hyphenated techniques, such as gas chromatography/ mass spectrometry with retention time locking (GC/MS/RTL), liquid chromatography/time-of-flight mass spectrometry (LC/ MS/TOF), micro fluidic-based capillary electrophoretic analysis of mitochondrial DNA (mtDNA), and laser ablation inductively coupled plasma mass spectrometry (LA/ICP/MS), are able to uncover forensically germane information by providing unprecedented levels of analytical selectivity and sensitivity

Track 18: Radio Analytical Techniques

Radio analytical Techniques focuses on analysis of sample for their radionuclide content. The Radio analytical Chemistry Capability (RACC) combines radioanalytical chemistry and medium level gamma-ray spectrometry. It has wide applications in the field of forensics, atmospheric sciences, health protection, archeology, and engineering.

Please contact the event manager Marilyn (marilyn.b.turner(at)nyeventslist.com ) below for:
- Multiple participant discounts
- Price quotations or visa invitation letters
- Payment by alternate channels (PayPal, check, Western Union, wire transfers etc)
- Event sponsorship

NO REFUNDS ALLOWED ON REGISTRATIONS
Prices may go up any time. Service fees included in pricing.
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25th International Conference on Organic & Inorganic Chemistry (cse) S

25th International Conference on Organic & Inorganic Chemistry


OrganicChem 2020

Conference Series LLC Ltd take great pleasure in welcoming academic scientists, researchers, research scholars, students and experts of application fields to Toronto, Canada for the OrganicChem 2020 Conference during April 12- 13, 2020 to foster the progress in the field by contributing with your expertise to what promises to be a very comprehensive and exciting meeting and to enjoy the immense unique artistic heritage and wonderful landscape of Toronto.
Details of OrganicChem 2020 Conference
Conference Name Place Date
OrganicChem 2020 Toronto April 12-13, 2020

 

OrganicChem 2020 is a global platform to discuss and learn about new compounds and its structure, bonding, reactivity in field of organic chemistry and organometallic chemistry, organic geochemistry, biogeochemistry, marine geochemistry, petroleum geochemistry, Bioorganic and medicinal chemistry. Advancement in fields of modern experimental organic chemistry, modern analytical organic chemistry, modern theoretical organic chemistry, combinatorial Chemistry, flow chemistry, green chemistry, microwave chemistry, microwave spectroscopy, new synthetic methods and advances in catalysis.

In the light of this theme, the Conference Series LLC Ltd aims to provide a forum for international researchers from various areas of chemistry, pharmacy, materials science and chemical engineering by providing a platform for critical analysis of new data, and to share latest cutting-edge research findings and results about all aspects of Organic Chemistry. The meeting will be a multidisciplinary gathering and present major areas such as organometallic, medicinal chemistry, polymer chemistry and overall applications.

Conference Series LLC Ltd organizes 1000+ Conferences Every Year across USA, Europe & Asia with support from 1000 more scientific societies and Publishes 700+ Open access journals which contain over 30000 eminent personalities, reputed scientists as editorial board members.

Target Audience

  • Organic Chemists

  • Inorganic Chemists

  • Professors in Chemistry

  • Associated and Assistant Professors in Organic Chemistry

  • Post-doctoral and Researchers in Chemistry

  • Heads of Chemical Departments

  • Post Graduates and Graduates in Medicinal Chemistry

  • Laboratory Chemists

  • Chemical Scientists working on Materials

  • Experts in the development of Organometallic Chemistry

 

Why to attend OrganicChem 2020??

The aim of the OrganicChem 2020 is to promote quality research and real-world impact in an atmosphere of true international cooperation between scientists and engineers by bringing together again the world class researchers, International Communities and Industrial heads to discuss the latest developments and innovations in the fields of Chemistry.

We sincerely hope that OrganicChem2020 serves as an international platform for meeting researchers from around the world, widen professional contact and create new opportunities, including establishing new collaborations.

We are looking forward to seeing you at OrganicChem 2020 in Toronto, Canada.


Conference highlights

  • Fundamental Concept of Organic Chemistry

  • Bioorganic and Biochemistry

  • Stereochemistry of Organic Compounds

  • Computational Chemistry and Cheminformatics

  • Phytochemistry and Pharmacognosy

  • Green Chemistry and Sustainable Technology

  • Polymers and Monomers

  • Bio-chemistry and agricultural chemistry

  • Analytical Chemistry

  • Advanced Synthesis and Catalysis

  • Physical Organic Chemistry

  • Natural Products and Heterocyclic Chemistry

  • Flow Chemistry

  • Medicinal Chemistry, Drug Synthesis

  • Inorganic and Bioinorganic Catalysis

  • Inorganic Materials and Nanoparticles

  • Organometallic Chemistry

  • Industrial Inorganic Chemistry

  • Organic Photochemistry

  • Forensic Chemistry

  • Modern Organic Chemistry and Applications

 

Market Analysis

The global chemical industry has grown by 7 percent annually, reaching €2.4 trillion in 2010. Most of the growth in the past 25 years has been driven by Asia, which now owns almost half of global chemical sales. The global chemical markets are expected to grow an average 3 percent in the next 20years. Asian players are positioned to own two-thirds of the market by 2030.

Organic chemical industry is anticipated to hold 51% of the total chemical industry market globally by 2030. With Asia Pacific, Europe, North America and Latin America being the leading markets for organic chemicals, the industry has witnessed approx. 10% growth in the last 5 years. Expanding industry applications, investment favouring industry policies are driving organic chemicals market till 2020.Extensive primary research is being conducted among leading companies such as BASF, Dow Chemicals, SABIC, Sinopec, and DuPont Chemicals and key opinion leaders from organic chemical industry.

Global Organic Acids Market was valued at $16,837 million in 2020, and is expected to reach $29,197 million by 2023, registering a CAGR of 8.3% from 2020 to 2023. Organic acids are weak acids that do not completely dissociate in water when compared to mineral acids.

Key players such as BASF SE, Cargill, Inc., The Dow Chemical Company, Eastman Chemical Company, Myriant Corporation, Celanese Corporation, Archer Daniels Midland Company, Henan Jindan Lactic Acid Technology Co. Ltd., Tate & Lyle Plc., and E. I. Du Pont De Nemours and Company have largely invested in R&D activities to develop advanced products to cater to the requirements of the consumers.

 

United States Chemical industry:

The chemical industry is one of the largest and most important industries worldwide. The United States is the largest national producer of chemical products globally. Including the pharmaceutical sector, its chemical output value was more than 767 billion U.S. dollars in 2020.

2020 ranking of leading United States chemical companies based on revenue (in billion U.S. dollars)

Projection of annual production growth in the United States chemical industry from 2020 to 2023

 

Canada Chemical Industry:

Canada’s chemistry industry is a world leader in low-intensity carbon chemical production for many reasons. Perhaps the biggest natural advantage the chemistry sector enjoys is access to abundant low-carbon fossil fuel feedstock. Natural gas is comprised of about 92% methane (CH4) and is used for heating fuel, electricity generation, and even as transportation fuel for vehicles with modified engines. Methane can also be a feedstock for some petrochemical manufacturing. Remaining components of natural gas are called natural gas liquids (NGLs) include ethane, propane, butane and pentanes. These are used as building blocks for plastics and solvents, polypropylene, refrigerants, rubbers and more.

A 2020 study from the Joint Research Centre of the European Commission compared different chemistry production processes and technological options to increase GHG efficiency and found that ethylene production that uses higher-carbon naphtha as a feedstock has an 82% higher GHG emissions factor than ethylene produced from lower-carbon ethane feedstock. Over the years, Canada’s chemistry sector has converted its ethylene facilities from naphtha to ethane feedstock and are already benefiting from this lower carbon approach to production.

Canada also has an abundant supply of low emissions hydroelectricity and huge potential for developing biomass resources to be used as feedstock and energy sources in chemistry production processes. With large portions of provincial energy grids already carbon-free, chlorine-related chemistries have a near-zero GHG footprint. In other countries, notably in Europe, Asia and the Middle East, high-carbon electricity grids result in higher GHG emissions associated with their chlorine production when compared to Canada.

 

United Kingdom Chemical Industry:

The UK industry is active in all key areas: basic inorganics, petrochemicals, polymers, agrochemicals, paints, detergents and personal care products, in specialties such as adhesives, flavours and fragrances, and in a host of industrial specialties including lubricants, fuel additives, construction chemicals and catalysts. It is also a global leader in pharmaceuticals. With £48.7 billion of revenues and £17.8 billion value added in 2020, chemicals & pharmaceuticals is the UK’s second largest industry. The current UK government has committed around £4.7bn to support R&D and innovation. This commitment should be seen against the broader ambition to boost R&D spending to 2.4% of GDP by 2027.

 

Sessions/ Tracks

1. Aspects of Organic Chemistry

Types and characterization of organic compounds
Functional groups
Aliphatic and aromatic compounds
Heterocyclic compounds
Nomenclature of new compounds
Efficiency in Organic Synthesis
Organic Synthesis for Materials Science
Organic Synthesis for Life Science

 

2. Bioorganic and Biochemistry

Classification of amino acids
Peptides sequence analysis
Stereochemistry of amino acids
Acid-Base behaviour of amino acids
Synthesis of amino acids
Reactions of amino acids
Peptide structure amino acid Analysis
Nucleosides
Classification of carbohydrates
Fischer projections and the DL notational system
Aldotetroses
Disaccharides and polysaccharides
Epimerization and isomerizations

 

3. Stereochemistry of Organic Compounds

Molecular chirality and enantiomers
Properties of chiral molecules and optical activity
The cahnIngoldPrelog RS notational system
Physical properties of enantiomers
Stereogenic center 

 

4. Computational Chemistry and Cheminformatics

Chemoinformatics and its applications
Cheminformatics tools for drug discovery
Quantitative structure activity relationship
Bioinformatics

 

5. Phytochemistry and Pharmacognosy

Natural products chemistry in drug discovery
Isolation and structure determination of natural products
Analysing pharmacogenomics studies
Phytotherapy
Herbs and botanicals as dietary supplements
Ethnopharmacy
Comparative phytochemistry, its history, concepts, applications and methods

 

6. Polymers and Monomers

Polymer structure and morphology
Polymer synthesis and polymer coating
Enzyme kinetics and thermodynamics of enzymatic reactions

 

7. Bio-chemistry and agricultural chemistry

Biochemistry and agrochemicals
Elementary calculus
Weed biology and control
Biochemistry and metabolism
Environmental management

 

8. Advanced Research in Environmental Organic Chemistry

Probes of Applied Science
Analysis of Semi and Volatile Compounds
Chemical Life Science
Environment Toxicology

 

9. Analytical Chemistry

Standardizing analytical methods
Equilibrium chemistry
Gravimetric methods
Titrimetric methods
Spectroscopic methods
Electrochemical methods
Chromatographic & Electrophoretic
Quality assurance
Additional resources

 

10. Advanced Synthesis and Catalysis

Heterogeneous catalytic process
Catalyst formulation and preparation methods
Catalysts characterization methods
Mechanism of catalytic reactions
Design of catalysts and simulation techniques

 

11. Physical Organic Chemistry

Atomic theory
Biophysical Chemistry
Thermochemistry and quantum chemistry
Chemical bonding, aromaticity, anti and homoaromaticity and structures
Solvent effects and isotope effects on organic reactions
Acidity, nucleophilicity and electrophilicity
Equilibria

 

12. Natural Products and Heterocyclic Chemistry

Chemistry and efficacy of natural products
Safety and regulations on natural products
Cosmeceuticals, nutraceuticals (functional foods) and beverages
Health and beauty product development and innovation
Methodologies for natural products

 

13. Flow Chemistry

Continuous flow reactors
Photo chemistry in combination with flow chemistry
Electrochemistry in combination with flow chemistry
Segmented flow chemistry

 

14. Combinatorial Chemistry

Parallel Synthesis of Combinatorial Chemistry
Application of Solid Phased Reagents
Diversity in Oriented Synthesis

 

15. Medicinal Chemistry, Drug Synthesis

Pharmaceutical Sciences
Drug discovery
Pharmacophore and Xenobiotic metabolism
Pharmacognosy and Pharmacokinetics
Pharmaceutical Industry
Anticancer agents
Pharmacology and toxicology
CADD (Computer Aided Drug Design)
Drug Design and Drug Development
Hit to lead and lead optimization
Synthesis and Medicinal Chemistry for Cancer and Age-Related Diseases
QSAR (Quantitative Structure-Activity Relationship) Fragment-Based Drug Design
Organic and Medicinal Chemistry Technologies for Drug Discovery

 

16. Inorganic and Bioinorganic Catalysis

Crystallography
Coordination Chemistry & Case Studies
Organometallic chemistry
Molecular geometry
Ligand field theory
Descriptive Chemistry
Electronic configurations
Crystal Lattices
Crystal Field Theory
Reactions in aqueous solutions

 

17. Inorganic Materials and Nanoparticles

Materials Science and Engineering
Polymer technology
Nanotechnology in material science
Mining, Metallurgy and Materials Science
Computational Materials Science
Electrical, Optical and Magnetic Materials

 

18. Organometallic Chemistry

Organometallic nomenclature
Carbonmetal Bonds in organometallic compounds
Grignard reagents
Transition metal organometallic compounds
Carbenes and carbenoids

 

19. Organic Industrial Chemistry

Quality Control of Crude Drug Materials
Petroleum and Petrochemicals Distillations
Assay Values of Crudes and its Reconfigurations
Organic Chemistry and its Clinical Diagnostics Techniques in Industries
Industrial pharmaceutics

 

20. Inorganic Industrial Chemistry

The Chemical Industry.
Sources of Inorganic Raw Materials
Sulfuric Acid and Sulfates
Nitrogen Compounds
Phosphorus Compounds
Chlor-Alkali Compounds
Titanium Dioxide

 

21. Modern Organic Chemistry and Applications

Organic synthesis
Development of synthetic methodologies
Functional organic materials
Supramolecular and macromolecular chemistry
Physical and computational organic chemistry
Heterocycles
Bioorganic Chemistry
Asymmetric Reactions
Metals in Organic Chemistry 
Graphene 
Nanostructures from DNA building blocks 
Tuberculosis diagnostics 
Fluorination 
Pyrrolysine
Structural biology by NMR.

 

OCM for OrganicChem Series Conferences

Organizing Committee - GOICC 2020

OCM Member

Kallol K. Ghosh

Professor
Pt. Ravishankar Shukla University, Raipur , India
India

 


OCM Member

Edward Lee Ruff

Professor
York University
USA

 


OCM Member

Yuichi Shimazaki

Professor
Ibaraki University
Japan

 


OCM Member

Maged Henary

Professor
Georgia State University 
USA

 


OCM Member

Mahesh N. Sanzgiri,

Professor
St. Xavier’s College
India

 


OCM Member

Romano VA Orru

Professor
VU University
Netherland

 


OCM Member

Majid M Heravi

Professor
Alzahra University
Iran

 


OCM Member

Waldemar Adam

Professor Emeritus
University of Puerto Rico
Puerto Rico

 


OCM Member

Jun Yin

Associate Professor
Georgia State University
United States

 


OCM Member

P. Gregory Van Patten

Department Chair
Middle Tennessee State University
United States

 


OCM Member

Xin-Tao Wu

Professor
Chinese Academy of Sciences
China

 


OCM Member

Yong-Li Zhong

Principal Scientist
Merck & Co., Inc.
USA

 


OCM Member

Saad Alotaibi

Dean of Turabah Abdullah university
Taif University
Kingdom of Saudi Arabia

 


OCM Member

Mariarosa Raimondo

Senior researcher
ISTEC CNR, Italy
Italy

 

Please contact the event manager Marilyn ([email protected] ) below for:

- Multiple participant discounts
- Price quotations or visa invitation letters
- Payment by alternate channels (PayPal, check, Western Union, wire transfers etc)
- Event sponsorships

NO REFUNDS ALLOWED ON REGISTRATIONS
Service fees included in this listing.
-----------------------------------------------------------------
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http://www.BostonEventsList.com
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MYL180913CEV

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32nd International Conference on Dental Science & Advanced Dentistry

32nd International Conference on Dental Science & Advanced Dentistry

About

Advanced Dentistry Conference 2020

Advanced Dentistry Conference:

Conference Series LLC Ltd welcomes all the participants from all over the world to attend 32nd International Conference on Dental Science & Advanced Dentistry which is going to be held in Chicago, USA during June 24-25, 2020. The theme of the esteemed event is “The art of dentistry” which will bring together Dentists, Dental professional, Dental Hygienists, Dental Students, Dental researchers, Dental Educators, Dental Business Leaders etc. from all over the world who are engaged in the field of Dentistry.

Conference Series LLC Ltd organizes 3000+ global events in a calendar year which includes International Conferences, Workshops, Exhibitions, and Symposia in all the important disciplines like Clinical, Medical Pharmaceutical, Management, Engineering etc.

What’s New?

Advanced Dentistry Conference-2020 includes international attendee workshops, lectures, and exhibitions, poster presentations including a designated registration area, a refreshment break, and gala lunch. Participants can join the Advanced Dentistry Conference 2020 as an international member to receive special benefits on registration packages. So come and join leading experts and eminent professionals to keep up with the pace of modern developing dentistry world will continue to in the future.

Target Audience:

· Dental Surgeons

· Principal Dentist’s

· Dental Nurses

· Orthodontists

· Periodontics

· Dentists

· Dental House Officers

· Dental and Oral Health Researchers, Faculty and Students

· Dental and Oral Health Associations, Societies and Universities

· Dental or Oral Hygienists & Therapists

· Dental Treatment Coordinators

· Dental Partners or Owners

· Dental Wholesalers, Dealers and Distributors

· Manufacturing Medical Devices Companies

· Dental Business/Practice Managers.

Sessions / Tracks

Track 1: Dental public health

Good dental or oral care is important to sustaining healthy teeth, gums and tongue. Oral problems comprising bad breath, dry mouth, canker or cold sores, TMD, tooth decay, or thrush are all treatable with proper diagnosis and care. Oral health is necessary to general health and well-being at every stage of life. A healthy mouth enables not only nourishment of the physical body, but also improves social interaction and promotes self-esteem and feelings of well-being.

Track 2: Endodontics

Endodontic is the division of dentistry that deals with infections of the tooth root, dental pulp, and adjacent tissue. Teeth are composed of a rigid structure surrounding a soft, living tissue called the pulp. The pulp comprises nerves, blood vessels and connective soft tissue. When the pulp become diseased or damaged and eventually dies, treatment will be essential to save the tooth. Root canal therapy is the most common technique done by an endodontist to remove the infested pulp and nerves from the tooth’s root canal. Other procedures include endodontic retreatment and endodontic surgery to prevent extractions.

Track 3: Forensic Odontology

Forensic odontology is the proper handling, examination and evaluation of dental evidence, which will be then presented in the interest of justice. The evidence that may be derived from teeth is the age (in children) and identification of the person to whom the teeth belong. This is done using dental records including radiographs, ante-mortem (prior to death) and post-mortem (after death) photographs and DNA. The other type of evidence is that of bite marks, left on either the victim (by the attacker), the perpetrator (from the victim of an attack), or on an object found at the crime scene. Bite marks are often found on children who are abused.

Track 4: Geriatric Dentistry

Geriodontics is the delivery of dental care to older adults involving the diagnosis, prevention, and treatment of problems associated with normal aging and age-related diseases as part of an interdisciplinary team with other health care professionals. The dental diseases that the elderly are particularly prone to are root caries, attrition, periodontal disease, missing teeth because of earlier neglect, edentulism, poor quality of alveolar ridges, ill-fitting dentures, mucosal lesions, oral ulceration, dry mouth (xerostomia), oral cancers, and rampant caries.

Track 5: Oral and Maxillofacial Surgery

Oral & Maxillofacial Surgery is the division of dentistry that comprises surgery to correct diseases, injuries and flaws in the head, neck, face, jaws and the hard and soft tissues of the oral and Cranio-maxillofacial region. The field of Oral & Maxillofacial Surgery varies from simple extractions and surgical removal of buried teeth to controlling of facial trauma. Typical oral surgical processes includes extraction of teeth, wisdom teeth surgery, dental extractions for physically compromised patients, placement of dental implants, bone grafting, tongue tie surgery , and analysis and treatment of cysts and tumors.

Track 6: Oral Implantology | Dental Conferences USA

Oral Implantology is intended to promote study and scientific research in the field of dental implantology and allied biomedicaz disciplines at Dental Dubai. It provides valuable information to general dentists, oral surgeons, prosthodontics, periodontists, scientists, clinicians, laboratory owners and technicians, manufacturers, and educators during Dentistry workshop and Dentistry conferences. Dental Implant basics, prosthetics, pharmaceuticals, and the latest research in implantology, implant surgery, and advanced implant procedures.

Track 7: Oral Cancer | Dental Conferences USA

Oral cancer can form in any portion of the mouth or throat. Most oral cancers begin in the tongue and in the floor of the mouth. Anybody can get oral cancer, but the threat is higher for male, over age 40, use tobacco or alcohol or have a past of head or neck cancer. Repeated sun exposure is also a risk for lip cancer. Oral cancer treatments may comprise surgery, radiation therapy or chemotherapy.

Track 8: Orthodontics

Orthodontics is the division of dentistry that deals with teeth arrangement to correct malocclusions and also the modification of facial growth. While orthodontic treatment has usually been suggested for functional reasons, it is increasingly used for aesthetic reasons to develop a person’s appearance. Typical problems corrected using orthodontic applications include improperly aligned teeth, crowded or irregularly spaced teeth, swelling teeth, extra or missing teeth, misaligned jaws and bite problems. Orientation problems could also have arisen through accidents , prolonged thumb sucking or pacifier sucking in grown-up children, missing teeth, premature or late loss of baby teeth, tumors in the mouth, dental disease or inadequately fitted fillings, crowns or braces.

Track 9: Pediatric Dentistry

Pediatric dentistry is the dental field that provides primary and widespread oral health care for children from infancy through youth and patients with special health care needs. Pediatric dental treatment and disease avoidance is provided for children up to 14 years of age, with special services for newborns and infants. Pediatric dentists encourage the dental health of children as well as help as educational resources for parents. Early detection is necessary to maintain oral health, modify unusual habits, and treat as needed and as simply as possible.

Track 10: Prosthodontics

Prosthodontics or prosthetic dentistry: is the part of dentistry that focuses on dental prostheses. Prosthodontists offer multi-disciplinary levels of care and offer the most progressive form of sequencing treatment, restorative treatment and maintenance. Prosthodontic treatments are designed to produce a balance between functionality, longevity and aesthetics, which include crowns and bridges, bonding and veneers, dentures, dental implants, and full mouth restoration.

Track 11: Veterinary Dentistry

Veterinary dentistry is the field of dentistry applied to the care of animals. It is the art and science of prevention, diagnosis, and treatment of conditions, diseases, and disorders of the oral cavity, the Maxillo-facial region, and its associated structures as it relates to animals. It is important to examine the whole animal, even when the primary complaint is the mouth. Some dental diseases may be the result of a systemic problem and some may result in systemic complications. In all cases, dental procedures require a general anesthetic so it is important to establish the cardiovascular and respiratory status and canine and feline physiological values of the patient to avoid risks or complications.

Track 12: Cosmetic Dentistry

Cosmetic dentistry states to any dental work that improves the appearance of a person's teeth, gums. It mainly focuses on enhancement dental aesthetics in color, position, shape, size, alignment and overall smile appearance. It involves the addition of a dental material to teeth or gums, removal of tooth structure or gums, straightening of teeth accompanied by an improvement in appearance of face.

Track 13: Restorative Dentistry

Restorative Dentistry is the study, analysis and integrated management of diseases of the oral cavity, the teeth and supporting structures. It comprises the rehabilitation of the teeth and the oral cavity to the functional, psychological and aesthetic necessities of the individual patient, including the coordination of multi-professional working to achieve these objectives. The focus of the Restorative Dentistry specialty is to work with other dental, medical and surgical specialists and other clinical associates, to provide and support the integrated management and oral rehabilitation of patients with complex treatment needs.

Track 14: Periodontics

Periodontics or Periodontology is the division of dentistry that deals with the management of the tissues surrounding and supporting the teeth, especially the gums. Gum cure is essential to prevent tooth loss. Common periodontal processes include scaling and root development, periodontal surgery, dental implants, and cosmetic techniques such as crown lengthening, soft tissue grafts, and ridge augmentation.

Track 15: Oral Appliance therapy

Oral appliance therapy is an effective cure option for snoring and obstructive sleep apnea (OSA). A custom-fit oral sleep appliance can recover sleep, restore alertness and rejuvenate health. Worn only during sleep, an oral appliance fits like a sports mouth guard or an orthodontic retainer. It supports the jaw in a forward point to help retain an open upper airway. Study shows that oral appliance therapy is an effective treatment preference for snoring and obstructive sleep apnea. The therapy is an effective, non-invasive treatment that fits easily into lifestyle.

Track 16: Sleep Apnea Syndrome

There are numerous types of sleep apnea, but the most common is obstructive sleep apnea. It is a potentially severe sleep disorder. It causes breathing to frequently stop and start during sleep. This type of apnea arises when throat muscles intermittently relax and block airway during sleep.

Track 17: 3-D imaging in dentistry

3D Imaging is one of the most significant tools for orthodontists to evaluate and record size and form of craniofacial structures. Orthodontists regularly use 2-dimensional (2D) static imaging procedures, but deepness of structures cannot be acquired and restricted with 2D imaging. Three-dimensional (3D) imaging has been developed in the early of 1990's and has gained a prized place in dentistry, particularly in orthodontics. In 3D diagnostic imaging, a series of anatomical records is gathered using certain technical equipment, processed by a computer and later presented on a 2D monitor to present the illusion of deepness.

Track 18: Orofacial Myofunctional therapy in dental practice

Orofacial Myofunctional Therapy It is neuro-muscular re-education of the oral facial muscles through a chain of exercises, to help in the normalization of the developing or advanced craniofacial structures and function. It is behavioral modification to eradicate dysfunctional practices. It works with the muscles of the lips, tongue, cheeks and face and their related purposes such as breathing, sucking, chewing, swallowing and speech as well as the rest position of the tongue and cheeks. It is used to form, balance, and stabilize, the stomatognathic and cranial systems.

Track 19: Dental Ethics

Ethics is a discipline dealing mainly with moral duty, conduct, and judgment. The dentist and the practice of dentistry are organized by many laws on the federal, state, and local level. Dental Ethics mean moral duties and obligations of the dentist towards his patients, specialists and associates and society. "Dentistry meetings" and Dentistry conferences help to encourage the welfare and equality of human beings.

Track 20: Dental Marketing

Dental market is a swiftly growing section with numerous products at different stages of clinical pipeline and others at different stages of industry life cycle. Disease incidences are escalating rapidly across the globe due to which high unmet demand has been formed and companies along with researchers are trying to provide effective medical care to patients. Dentistry congress, Dentistry workshops and Dentists Meeting delivers the good platform for the dental practice business aspects.

Please contact the event manager Marilyn (marilyn.b.turner(at)nyeventslist.com ) below for:
- Multiple participant discounts
- Price quotations or visa invitation letters
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- Event sponsorship

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2nd International Conference on Plastic & Cosmetic Surgery (CSE) AS

2nd International Conference on Plastic & Cosmetic Surgery

About

Plastic Surgery 2020

Details of Plastic Surgery Conference in Chicago

Conferenceseries LLC Ltd is organizing Plastic Surgery in 2020 at Chicago, USA. The Conference is mainly focuses on the latest and exciting innovations in every area of Plastic Surgery, Cosmetology, Re-constructive surgery.



Conference Name


Place


Date

Plastic Surgery 2020


Chicago, USA


August 02-03, 2020

We are glad to announce the inception of the 2nd International Conference on Plastic & Cosmetic Surgery, going to be held at Chicago, USA, during August 02-03, 2020.

Conference Series LLC Ltd is an open resource platform that conducts 3000+ global events including International Conferences, Workshops, Symposia, Trade Shows, Exhibitions and Science Congresses in all the major scientific disciplines, including Clinical, Medical, Pharmaceutical, Engineering, Technology, Business Management and Life Sciences across America, Europe, The Middle East, and Asia Pacific. It is reaching over 25 million researchers, scholars, students, professionals and corporate entities all over the globe.

Why to Attend??? 

In this modern era of technology with individuals throughout the globe has eagerly trying finding out latest innovations about the Plastic and Cosmetic Surgery and the equipments, this is the best chance for individual to achieve the biggest gathering of members and interchanging knowledge. Get the top market leaders in plastic surgery equipments and technology, meet with present and potential clients, make a sprinkle with another product offering, and get name acknowledgment at this 2-day occasion.

Why Chicago???

Here are some key reasons why Chicago:

Chicago has occupied the six places in the Best Student Cities this year.
Chicago is ranked 40th in 2020 and is in the top 10th for the ranking indicator
It is the home to one of the top 10 universities in the world rankings.
Chicago is also one of North America’s best cities for creative
Many attractive tourist spot are there in Chicago like Museum of Science and Industry, Millennium Park, Art Institute of Chicago and so on.

Conference Highlights:

Facial Surgery

Breast Surgery

Cosmetic & Aesthetic Surgery- Minimally Invasive

Body Lift

Medical devices and equipment

Oral and maxillofacial surgery

Hand Surgery

Gender Reassignment Surgery

Burn Care / Trauma Surgery

Pediatric plastic surgery

Market Analysis

Global Plastic Surgery Market Report

Plastic surgery in it’s broader sense is to restore and enhance of the aesthetic appearance of an individual. Plastic Surgery can be broadly segmented in two based on the purpose of surgeries; reconstructive surgery and Aesthetic procedures & Cosmetic surgery. : Reconstructive Surgery in it’s broader sense, is to reconstruct parts of body parts. It can be classified into various sectors like Nose( Rhinoplasty), eye lid (Blepharoplasty), tummy tuck(Abdominoplasty) and so on. Aesthetic surgery includes in altering the appearance of a body part. While a patient has no choice in case of reconstructive surgery, aesthetic surgery can be the light in the dark.

As per the market research of 2020 by Market research Future, the market for cosmetic surgery is expected to reach $ 21.97 billion by the end of with CAGR of ~7.8% during 2020-2023.

US Cosmetic Surgery Market 2020:

The market growth Factors :

There are several growth factors for the market growth of Plastic & Cosmetic Surgery :

Health factors : With the rise of technology we are facing several health issues like obesity, accidents and many more which is one of the main growing factors of Cosmetic Surgery market.
Social and cultural factors : Social impact is also one of the main growth factor to increase the market of Cosmetic Surgery. There are many impacts such as influence of media, fashion and film industry, peer pressure for appearance and beauty, changing dimensions of beauty etc.
Technological factors : With the development of technology, we are moving one by one steps towards advancements, with the flow of technology we are also changing our self with the development of advanced materials like silicone implants and so on.

Economic factors : Now day by day the income per capita is increasing, it is also a key growth factor for the high cost cosmetic surgeries.



There are also some factors which can be threaten for the growth of Cosmetic surgery market :

Non-essential nature of cosmetic surgery.
Social taboos against violation of body parts.
High cost of cosmetic surgeries despite reduction.
Lack of skills to perform the procedures, which can be due to the market needs of providing all the procedures in a single clinic.

As per the plastic surgery statistics released in 2020 by ISAPS- International society of aesthetic and plastic surgery, the increase in procedures show the potential in the global market of plastic surgery.

By 2020, the worldwide market for aesthetic/reconstructive surgeries will be $10.7 billion.
The U.S. and the Latin America markets are expected to have a CAGR of 10%, respectively, of 9.2% and 10%.
The USA market holds more than 45% of the market.
For Europe it has observed s relatively slower growth of 6.6% per year. The reason includes the declining purchasing power, particularly in southern Europe.
The future growth of European market is 6.6% and reach $1.94 billion by 2020.
For the Asia Pacific region it have an overall CAGR of more than 14.1% with increasing demand.
Aesthetic and Reconstructive product market also has a high growth in China, Japan and South Korea due to the expanded access of technology. Europe market will reach $2.24 billion by 2020.
The global plastic surgery instruments market is expected to reach $1,479.0 Million by 2023 presently in 2918 it is $1,002.0 Million at a CAGR of 8.1%.
The international market of medical aesthetic treatment is expected to reach upto US$6.56bn by 2020.



Global Asthetic and Surgical Market year wise :



Key players of Global Cosmetic Surgery Market:

Johnson & Johnson
Valeant Pharmaceuticals International
Cutera Inc.
Syneron Medical Ltd
Allergan Inc.
Genesis Biosystems lnc.

Please contact the event manager Marilyn (marilyn.b.turner(at)nyeventslist.com ) below for:
- Multiple participant discounts
- Price quotations or visa invitation letters
- Payment by alternate channels (PayPal, check, Western Union, wire transfers etc)
- Event sponsorship

NO REFUNDS ALLOWED ON REGISTRATIONS
Prices may go up any time. Service fees included in pricing.
-----------------------------------------------------------------
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9th International Conference on Pharmaceutical GMP, GCP & Regulatory Affairs

9th International Conference on Pharmaceutical GMP, GCP & Regulatory Affairs

About

2020 Key ThemesRegulatory Affairs 2020 conference will focus on new strategies, amendments, innovations, developments in the fields of regulatory affairs, intellectual property rights and medical devices with the theme: “Current challenges of Pharmaceutical & Biopharmaceutical Industries in regulatory framework” which reflects new strategies in the field of regulatory affairs. This conference includes workshops, symposiums, special sessions, key note sessions, conducted by eminent and renowned speakers who excel in the field of regulatory affairs, medical devices, intellectual property rights which include the topics regulatory affairs in pharmacovigilance, clinical affairs & regulatory strategies, regulatory strategies and developments, penalties of regulatory Non-compliance, biologics & biosimilars, global regulatory intelligence, Impact of Brexit on regulatory framework, regulatory requirements in pharmaceuticals, regulatory challenges for medical devices, medical device and combination products regulation, Intellectual property rights etc. This International Regulatory Affairs Conference also encourages the active participation of Young Researchers, Students as we are hosting Poster Award Competition and Young Research Forum at the conference venue.

Product Registration & Submission
Global Guidelines for the Development of Biologics
Medical Device & Combination Products Regulations
Accelerating Approval of New Drugs
ASEAN Labelling Harmonisation
Regulatory & Clinical Affairs
Regulatory & Pharmacovigilance
Regulatory Enforcement & Inspection

Target Audience:

Regulatory Affairs experts
Clinical Research Associates
Medical Devices experts
Quality Assurance experts
Intellectual Property Rights attorneys
Scientists
Researchers
Academicians
Industrialists

Continent wise participation Analysis for Regulatory Affairs 2020 conference

Session/Tracks

Track 1: Regulatory Affairs

Regulatory Affairs profession was developed by the government regulatory bodies to regulate the safety and efficacy of products to protect the health of public. This was developed in all most all divisions of health care industry like pharmaceuticals, veterinary medicines, medical devices, pesticides, agrochemicals, cosmetics, complimentary medicines etc. This profession involves development of new and existing products from early on, preparation and till submission to the relevant regulatory bodies of health authorities by inputting regulatory principles.

Regulatory Affairs is involved actively from early stage of development to post marketing activities of new and existing products. This department is one of the integral parts within the organization structure of pharmaceutical industry. Internally it collaborates at the interphase of drug development, manufacturing, marketing and clinical research. Externally it is the key interface between the commercial industry which undergoes drug development to clinical research and the regulatory authorities.

Track 2: Regulatory Affairs in Pharmacovigilance

Regulatory Affairs (RA), likewise called government issues, are a calling inside managed enterprises, for example, pharmaceuticals, medicinal gadgets, vitality, saving money, telecom and so on. Administrative Affairs likewise has a certain importance inside the human services enterprises (pharmaceuticals, therapeutic gadgets, biologics and useful nourishments). Administrative issues (therapeutic issues) experts (otherwise known as administrative experts) typically have duty regarding the accompanying general territories.

Pharmacovigilance evaluates the adverse effects in turn speaking about the efficacy and safety data of particular drug product thus, collaboration of pharmacovigilance with regulatory bodies provides all the adverse reactions, safety data to regulatory authorities.

Working with government, state and neighborhood administrative offices and faculty on particular issues influencing their business i.e., working with so much office as the Food and Drug Administration or European Medicines Agency (pharmaceuticals and restorative gadgets); The Department of Energy; or the Securities and Exchange Commission (banking). Advising their organizations on the administrative angles and atmosphere that would influence proposed exercises. i.e., portraying the "administrative atmosphere" around issues, for example, the advancement of professionally prescribed medications and Sarbanes-Oxley consistence.

Track 3: Clinical Affairs & Regulatory Strategies

An administrative science driven administrative procedure is crucial as a component of today's biopharmaceutical item early advancement arranging. An all-around arranged administrative methodology will adjust the proposed clinical advancement arrangement with business targets, and pre-emptively distinguish challenges, and also, proposed elective/creative ways to deal with new item improvement which influence new measures for confirmation era supporting proceeding with improvement and worldwide business sector approval. An administrative methodology characterizes key issues/difficulties to proactively talk about with Regulatory powers furthermore characterizes key system points of reference that are frequently considered business impetuses driving speculator intrigue and financing. In particular, an auspicious, very much arranged and all around kept up administrative technique, with proactive and collective cooperation with administrative powers, is regularly a separating element for industry pioneers putting up monetarily fruitful and creative items for sale to the public in today's aggressive commercial center. Administrative procedure is a noteworthy segment of fruitful biopharmaceutical item improvement. Covance Global Regulatory Affairs gets ready and keeps up administrative science driven and item particular worldwide administrative systems for some item sorts, e.g., drugs, biologics, drug-gadget mixes, antibodies, quality treatments, cell-treatments, over a scope of restorative territories and full administrative technique support for item improvement activities.

Track 4: Regulatory Strategies and Developments

Regulatory strategies are formal documents that include series of regulatory activities to discover an innovative product or a modified product to market with business strategy for that product. This provides description and course to project team for the product being developed with identification of important regulatory elements which are addressed to market the product. Within a firm there are many regulatory strategists from different departments that involve all aspects of a drug and individuals with expertise in chemical synthesis, toxicology, biology, clinical and regulatory affairs, marketing, government affairs and reimbursement inputs into the regulatory strategy ensuring it is comprehensive.

Regulatory strategy document has three purposes, it acts as a:

A tracking tool to summarize key agreements reached with health authorities
A planning tool that documents timelines and lists topics to address in future meetings with health authorities
A risk register to record key issues that could impact timelines, costs or commercial value for the project

Track 5: Penalties for Regulatory Non-compliance:

Non-compliance costs are costs which result from a failure to comply with regulation. These costs are not considered to be part of the regulatory burden for the purposes of the Risk Based Monitoring. This includes penalties and activities associated with those penalties that are required to be undertaken because of noncompliance with regulation. Regulatory impacts that arise, up to the point that action is taken to respond to the suspicion of a specific instance of noncompliance, are included in RBM framework. This includes risk based frameworks that may target certain populations without a specific instance of suspicion. Failure to comply with the law can lead to enforcement action including one or more of the following: on-the-spot fines, prosecution, which carries a maximum fine of $12,110, disciplinary action, ranging from fines to cancellation of the license.

Track 6: Biologics & Biosimilars

A biopharmaceutical, otherwise called a biologic therapeutic item or biologic, is any restorative item made in, extricated from, or semi orchestrated from organic sources. Not quite the same as synthetically incorporated pharmaceuticals, they incorporate immunizations, blood, or blood segments, allergenic, substantial cells, quality treatments, tissues, recombinant restorative protein, and living cells utilized as a part of cell treatment. Biologics can be made out of sugars, proteins, or nucleic acids or complex mixes of these substances, or might live cells or tissues. They are confined from normal sources—human, creature, or microorganism. Phrasing encompassing biopharmaceuticals fluctuates amongst gatherings and elements, with various terms alluding to various subsets of therapeutics inside the general biopharmaceutical class. Some administrative offices utilize the terms natural restorative items or remedial organic item to allude particularly to designed macromolecular items like protein-and nucleic acid–based drugs, recognizing them from items like blood, blood segments, or antibodies, which are typically extricated specifically from a natural source Gene-based and cell biologics, for instance, frequently are at the front line of biomedical research, and might be utilized to treat an assortment of therapeutic conditions for which no different medications are accessible.

Track 7: Global Regulatory Intelligence

Ever-proliferating and changing global regulations generate complex challenges of execution in global market clearance operations.

Mission-critical decisions are delayed, trapping new international revenue until market clearance process issues are resolved. Workflow is confounded as information conflicts from sales-focused distributors, newly-appointed foreign regulators, and legacy resources are reconciled- and as definitive answers are sought. Governance is compromised as information gaps reduce assurance levels and impair risk management of clearance-related penalties, fines, and legal costs.

And the high level of business performance required to create value from ongoing medtech industry consolidation is not achievable, since global market clearance operations are incapable of rapidly completing new market clearance submissions for newly-acquired product lines.

Unlike repackaged RI databases designed for the pharmaceutical industry, the clinivation Worldview Enterprise Solution for On-Demand Global Regulatory Intelligence accelerates the market clearance cycle.

Track 8: Impact of Brexit on Regulatory Framework

The most important piece of UK legislation that would need to be repealed is the European Communities Act 1972 (ECA), which provides for the supremacy of EU law. Repealing the ECA will bring an end to the constitutional relationship that exists between EU and UK law. Moreover, the vast amounts of secondary legislation that have been passed with the objective and justification of implementing EU law would have to be considered by the Government. EU Regulations rely on the principle of direct applicability, which means that unlike EU Directives, they are directly implemented into UK law without the need for legislation from the UK Parliament. In this light, Regulations are more powerful legislative tools for the EU because of their immediate applicability. The status of existing Regulations will be addressed in the Great Repeal Bill, although as noted above, in many cases amendments will likely be needed to take into account the UK’s new relationship with the EU. The Court of Justice of the European Union (CJEU) situated in Luxembourg is the final arbiter on questions of the interpretation of EU law. In her first speech setting out the UK Government’s priorities for Brexit on 17 January 2020, the Prime Minister restated her position that the UK is not prepared to continue to be subject to the jurisdiction of the CJEU.

Track 9: Regulatory Communications and Submissions

Due to the growing interest in marketing new products, it is pivotal to establish a superior level of medical writing and regulatory operations. Executives within these roles need to create and manage successful submissions, as well as streamline timelines, to accelerate approval.

Attending the Optimizing Regulatory Communications and Submissions conference will aid delegates in expediting the approval of drugs while meeting requirements for different regulatory agencies worldwide. In addition, attendees will overcome key operational challenges impacting the approval process to enhance the quality of submissions.

Track 10: Marketing Authorizations-Affordable Healthcare and Fair Trade

This establishment level module is the perfect acquaintance for new participants with the field of pharmaceutical administrative issues and consistence. It portrays the central prerequisites that must be fulfilled to pick up and keep up endorsement to advertise restorative items in the USA and Europe. The lawful structure and the parts of significant players in control are displayed. The life-cycle of a medication is sketched out. The different systems accessible for appraisal and endorsement of items are depicted and their prerequisites laid out. Commitments to be satisfied in the wake of promoting endorsement are examined. Worldwide administrative undertakings bunches in industry give around the world, key initiative in and far reaching course of the legislature administrative necessities for item presentation and commercialization, using administrative learning to guarantee consistence and administrative knowledge and make open doors in an exceedingly controlled environment. The worldwide administrative undertakings bunch has vital and operational capacities, requiring accuracy and faultless execution, as an organization's prosperity depends on, partially, the direction and thorough appraisal gave by the administrative issues group. The key item advancement, assembling and enlistment turning points, (for example, Investigational New Drug documenting, end of stage II, stage III, New Drug Application entries, administrative office audit timetable and item endorsements), which are the corporate valuation and choice focuses, depend on basic administrative interface goalposts and developments. This underscores the significance of key administrative commitment to the business. Keeping in mind the end goal to be profitable donors and basic business accomplices, the worldwide administrative undertakings association must create instruments and build up frameworks to guarantee it has the right individuals and ability, capable procedures, productive profitability, sensational execution and accuracy in arranging.

Track 11: Regulatory Requirements for Pharmaceuticals

The new medication endorsement process have been made into three stages for improvement in comprehension - the principal stage is pre-advertising implied for revelation, advancement and clinical concentrates, second stage for promoting approval of medication and third is for post showcasing. Firstly, preclinical investigations of a medication are finished to guarantee adequacy and security, and after that application for behavior of clinical trials is submitted to the CDSCO. From that point, the clinical trials can be led (stage I to stage IV). These studies are performed to guarantee the viability, wellbeing and upgrading the measurements of medication in people. After the culmination of clinical investigations of the medication, then an application to the skilled power of India for the endorsement of medication for advertising is submitted. The able power audit the application and affirm the medication for advertising just if the medication is observed to be sheltered and successful in individual or the medication have more alluring impact as contrast with the danger.

Track 12: Regulatory Challenges for Medical Devices

As therapeutic gadget quality certification and administrative undertakings experts, it can test to remain focused of changes occurrence in our industry. Administrative controls for restorative gadgets are rare in the creating scene, despite the fact that usage of national medicinal gadget directions will frequently address the very issues brought up in nations as significant attentiveness toward patient wellbeing. Case of these issues incorporate the unlawful re-preparing and re-bundling of utilized syringes for re-deal; the accessibility available of hardware that fizzles least quality and security benchmarks; or just no hint of what gadgets are being sold in the nation, nor by whom. Such a posting is crucial to empower governments to issue cautions or reviews for perilous or inadequate things.

Track 13: Medical Device & Combination Products Regulations

Blend items are remedial and indicative items that consolidate medications, gadgets, and/or organic items. FDA hopes to get expansive quantities of blend items for audit as innovative advances keep on merging item sorts and obscure the verifiable lines of partition between FDA's therapeutic item focuses, which are comprised of the Center for Biologics Evaluation and Research (CBER), the Center for Drug Evaluation and Research (CDER), and the Center for Devices and Radiological Health (CDRH). Since mix items include parts that would regularly be controlled under various sorts of administrative powers, and much of the time by various FDA Centers, they raise testing administrative, strategy, and audit administration challenges. Contrasts in administrative pathways for every part can affect the administrative procedures for all parts of item improvement and administration, including preclinical testing, clinical examination, showcasing applications, assembling and quality control, antagonistic occasion reporting, advancement and promoting, and post-endorsement alterations.

Track 14: Best Industry Practices

Drug business is one in everything about nation's most critical monetary motors, trade $15 billion in stock yearly and a couple of its processing plants region unit preeminent. The government office has built up a progression of tips for creating GXP (which incorporates GCP, GLP and GMP directions) that shield each the life sciences business furthermore the clients they serve. In order to help FDA-directed firms, expert control offers partner in incorporated quality and consistence administration code that guarantees GLP, GCP and GMP rules consistence. Industry practices is likewise some portion of value danger administration framework, Pharma Regulatory Affairs, Audits and assessments, acceptance strategies (process approval and expository approval), Qualification, acceptance, adjustment, upkeep, hazard investigation Drug Safety and Good Pharmacovigilance hones. Some of our product framework applications which will encourage with GLP GCP GMP rules epitomize the resulting arrangements: Document Control/Document Management, Corrective Action Preventive Action (CAPA), alteration administration, guiding Management, resistance Automation programming framework, Audit Management in venture with GLP GCP GMP rules, customer protests programming framework, shapes based strategy robotization, electronic entries.

Track 15: Intellectual Property Rights

In the EU, an organic thoughtful item is one amongst the dynamic substance(s) made from or separated from a natural (living) framework, and requirements, also to physico-compound testing, natural testing for full characterization. The characterization of a natural medicative item could be a blend of testing the dynamic substance and hence the last medicative item along the edge of the get together strategy and its administration. Central thoughts of Intellectual Property Management (IPM) and its significance is a goad to human force and in this manner is the headway of financial and social improvement. It furthermore gives defense on the occasion Associate in usage of an IPM technique together with the administration of material ownership (IP) in a web setting. Investigative control law more often than not gives the creator of partner in scholarly creation restrictive rights for abusing and taking advantage of their creation. Experimental order insurance is intended to fortify the force of the human personality for the upside of all by verifying that benefits got from misusing a creation advantage the maker. This may energize action and allow financial specialists in investigation and improvement a decent go ahead their speculation. Experimental order presents on individuals, undertakings or option elements the right to bar others from the vocation of their manifestations wellbeing and quality control in naming. Therefore, material ownership rights (IPRs) could have an on the spot Associate in generous effect on exchange on the grounds that the proprietor of an IPR could - through the social control of such a privilege - prevent the assembling, use or offer of an item which incorporates the IPR. Therefore administration over the immaterial (IPR) suggests administration of the stock and markets. Exploratory order security energizes the production, conveyance and discourse demonstration of the creation to the overall population, rather than keeping it mystery though at indistinguishable time urging mechanical endeavours to choose imaginative works for abuse. Material ownership lawful titles identifies with the securing and utilization of an assortment of rights covering totally distinctive type of manifestations. Licenses in the pharmaceutical business incorporate both lawful and moral issues.

Please contact the event manager Marilyn (marilyn.b.turner(at)nyeventslist.com ) below for:
- Multiple participant discounts
- Price quotations or visa invitation letters
- Payment by alternate channels (PayPal, check, Western Union, wire transfers etc)
- Event sponsorship

NO REFUNDS ALLOWED ON REGISTRATIONS
Prices may go up any time. Service fees included in pricing.
-----------------------------------------------------------------
This event is brought to you by:
Conference Series - NewYorkEventsList
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Conference on Pharmaceutical Analysis & Analytical Chemistry (cse) AS

2nd International Conference on Pharmaceutical Analysis & Analytical Chemistry

 


Pharmaceutical Analysis 2020

 

After the fruitful execution of the International Conference on Pharmaceutical Analysis and Quality Control Strategies, Conference Series with great pride and honour announcing its International Conference on Pharmaceutical Analysis & Analytical Chemistry which is going to held in Chicago, USA during August 02-03, 2020.

Pharmaceutical Analysis 2020 serves as a podium for the interaction between experts in the area of pharmaceutical analysis and analytical chemistry around the world. We cordially invite all the eminent researchers, academicians, students, industry representatives working in these exciting areas.

This Conference is mainly focused on the theme “New paradigms in Pharmaceutical Analytical Techniques”. The conference includes workshops, symposiums, special keynote sessions conducted by eminent and renowned speakers who excel in the field of Pharmaceutical Analysis and Drug Discovery This International Pediatric Conference also encourages the active participation of young student researchers as we are hosting Poster Award Competition and Young research Forum at the conference venue.

Target Audience:

  • Pharmaceutical Analysis Researchers

  • Analytical Chemists

  • Noble Laureates

  • Directors, Presidents, CEO’s of Organizations/Companies

  • Pharmaceutical Associations and Societies

  • Academicians (Professors, Associate & Assistant professors, Deans, Directors)

  • Graduates and Post graduates

 

Sessions/Tracks

Track 1: Modern Pharmaceutical Analysis

Generally, Pharmaceutical Analysis alluded to the synthetic examination of medication atoms. Be that as it may, throughout the years, present day pharmaceutical investigation has advanced past this to envelop mix systems, high-throughput innovations, chemo metrics, micro dosing studies, scaling down and nanotechnology. These logical advances are currently being utilized in all phases of medication disclosure and the concentration of this survey will be on how these advances are being utilized inside this procedure. With new, enhanced and advancing innovations, and in addition new applications for existing innovation, the scan for new medications for the aversion and treatment of human maladies proceeds.

 

Track 2: Chromatography & Separation Techniques

Chromatography strategy for isolating the parts, or solutes, of a blend on the premise of the relative measures of every solute appropriated between a moving liquid streams, called the versatile stage, and a touching stationary stage. The versatile stage might be either a fluid or a gas, while the stationary stage is either a strong or a liquid. Increase in advances in Biotechnology sector augments the production of variety of valuable bio products. Molecules such as therapeutic proteins, enzymes, and other important products require combination of chromatography so as to purify them in purest form. Combination of these novel technologies minimizing the purification steps plays a crucial role for getting maximum purification of the biomolecules.

 

Track 3: Analytical Method Development and Validation

Analytic method development and validation are persistent and interconnected exercises directed all through the drug development process. The act of validation checks that a given method measures a parameter as planned and sets up the execution furthest reaches of the estimation. Albeit clearly conflicting, approved methods create comes about inside known vulnerabilities. These outcomes are essential to proceeding with drug development, as they characterize the rising learning base supporting the product. The time and exertion that are put into growing logically solid, hearty, and transferrable analytic methods ought to be lined up with the drug development arrange. The assets that are consumed on method validation must be constantly balanced with regulatory requirements and the likelihood for product commercialization.

 

Track 4: Spectroscopy and its Techniques

Spectroscopy deals with surplus of different techniques that employ electromagnetic radiation on materials in order to measure and interpret data, which is used for elucidating a variety of analytical problems. It includes absorption, emission, or scattering of electromagnetic radiation by atoms or molecules. Types of spectroscopy are IR & NIR, UV/visible, NMR, Atomic Emission Spectroscopy, Fluorescence Spectroscopy etc. Spectroscopic methods are used for Environmental Analysis, Biomedical studies, astronomy. UV-Visible Spectrometer is used for a varied range of applications.

 

Track 5: Pharmaceutical and Biomedical Analysis

Analytical biochemistry is the study of biochemical components found in a cell or other biological sample. This field uses a broad vary of techniques for separation, identification, quantification and practical characterization of biological molecules like nucleic acids, enzymes, proteins, pigments, carbohydrates and additional. The main ways involved in analytical biochemistry to separate the biological components are qualitative analysis techniques, chromate graphical Techniques, super molecule Estimation & Purification Techniques and medicine Techniques.

 

Track 6: Mass Spectroscopy: Approaches and Challenges

New mass spectrometry (MS) methods, collectively known as data independent analysis and hyper reaction monitoring. Last decade has witnessed remarkable technological advances in mass spectrometry based proteomics and Biologics. Specific advances include high throughput protein identification by multidimensional chromatography, automated tandem mass spectrometry and sequence data base searching, accurate quantification by the application of stable isotope dilution theory to protein analysis, and the targeted isolation of selected analytes by the use of highly selective chemistries.

 

Track 7: Bioanalysis

Bioanalysis involves the quantitative measurement of xenobiotics (drugs and their metabolites, and biological molecules in unnatural locations or concentrations) and biotics (macromolecules, proteins, DNA, large molecule drugs, metabolites) in biological systems. In the past two decades, has seen increase in the field of Biopharmaceuticals. Bioanalysis applies to the drugs used for anti-doping testing in sports, illicit purposes and Environmental concerns. The most frequently used techniques are liquid chromatography coupled with tandem mass spectrometry (LC–MS/MS) for micro molecules and enzyme-linked immunosorbent assay (ELISA) for macromolecules.

 

Track 8: Electro chemical and Thermo analytical techniques

Electrochemical Analysis is a powerful technique that is increasing in utility in the Pharmaceutical Industry due to its high sensitivity, speed of analysis, reduction in solvent and sample consumption, and low operating cost compared to other analytical methods. The modern Electrochemical Analytical techniques are cyclic, linear sweep, differential pulse, square wave and stripping voltammetric techniques. Thermo Analytical techniques are mainly used to detect compound purity, polymorphism, solvation, degradation, and excipient compatibility. It is extensively used in conducting Preformulation studies.

 

Track 9: Analytical Chemistry

Analytical Chemistry has many applications in Forensic Sciences, environmental analysis, and materials analysis. Analytical Chemistry research is mainly driven by the performance and cost. In these days, great efforts are being put to shrinken the analytical techniques to chip size. In this technology, the most used technique is lab-on-a-chip. The ongoing developments of computer automation and information technologies have broadened the analytical chemistry into a number of new biological fields.

 

Track 10: Preformulation Studies

Preformulation is considered as critical decision-making tool during both – drug discovery and development phase. Preformulation studies help in assessing the drugability of a molecule. To generate Preformulation data analytical techniques like Spectroscopic, Chromatographic, Thermal methods and some specific detection methods like Capillary electrophoresis are used.

 

Track 11: Hyphenated Techniques in Analytical chemistry

Hyphenated technique is developed from the coupling of a separation technique and an on-line spectroscopic detection technology. These techniques are mainly broadened their applications in the analysis of natural products.

 

Track 12: Quality Assurance and Quality Control

Quality assurance is defined as a procedure or set of procedures intended to ensure that a product or service under development meets specified requirements. Quality control (QC) is a procedure or set of procedures intended to ensure that a manufactured product or performed service adheres to a defined set of quality criteria that meets the requirements of the client or customer. The two approaches can be thought of simply as failure detection (QC) and failure prevention (QA). The ISO 9000 family of quality management systems standards is designed to help organizations ensure that they meet the needs of customers and other stakeholders while meeting statutory and regulatory requirements related to a product or service.

 

Track 13: Pharmaceutical Analysis Errors and Validation

Analytical errors are fundamental before submitting your report and results with the required level of confidence. However, we should have clarity regarding accuracy and precision before we are talking pharmaceutical error. Most of us believe that these terms have the same meaning but the example of arrows striking a target. Any measurement is limited by the precision of the measuring instruments and the technique and the skill of the observer. Where a measurement consists of a single reading on a simple piece of laboratory equipment, for example, a burette or a thermometer, one would expect the quantity of factors adding to vulnerabilities in that estimation to be less than an estimation which is the consequence of a multi-step process comprising of at least two weight estimations, a titration and the utilization of an variety of reagents.

 

Track 14: GLP and GMP Method Development, Validation and Remediation

Good manufacturing practice is the piece of quality assurance which ensures that things are reliably made and controlled to the quality standard proper to their proposed use and as required by the Marketing Authorization or item particular. GMP is stressed over both generation and quality control, consistency with this standard gives open assurance that the rights, security, and prosperity of trial subjects are ensured; predictable with the rule that have their starting point in the Declaration of Helsinki, and that the clinical information is valid.

 

Track 15: Biosensors

Biosensor is a device which converts the information regarding the presence of a compound into electro analytical Signal. The biosensor research areas include modern Bio specific analytical techniques. In the recent years, micro fabrication techniques have showed a significant improvement in biosensor systems. The modern methods of the biosensor discoveries range from electrochemical, electromechanical, and fluorescence-­cum-optical-based biosensors and genetically engineered microbes.

 

Track 16: Pharmaceutical Microbiology

Modern microbiology is unmistakably a branch of biotechnology and incorporates the customary and nucleic corrosive aspects. Pharmaceutical microbiology is the connected branch of microbiology which enables drug specialists to make pharmaceuticals from microorganisms either straightforwardly or with the utilization of some item delivered by them. Different parts of pharmaceutical microbiology incorporate innovative work for assembling of different hostile to tumours, against microbial specialists.

 

Track 17: Forensic Analysis

Multiply hyphenated techniques, such as gas chromatography/ mass spectrometry with retention time locking (GC/MS/RTL), liquid chromatography/time-of-flight mass spectrometry (LC/ MS/TOF), micro fluidic-based capillary electrophoretic analysis of mitochondrial DNA (mtDNA), and laser ablation inductively coupled plasma mass spectrometry (LA/ICP/MS), are able to uncover forensically germane information by providing unprecedented levels of analytical selectivity and sensitivity

 

Track 18: Radio Analytical Techniques

Radio analytical Techniques focuses on analysis of sample for their radionuclide content. The Radio analytical Chemistry Capability (RACC) combines radioanalytical chemistry and medium level gamma-ray spectrometry. It has wide applications in the field of forensics, atmospheric sciences, health protection, archeology, and engineering

 

Why to Attend

Pharmaceutical Analysis will provide you a great opportunity to meet with like-minded people and industry peers. This is the best place to present your research in front of the global audience coming from the different countries. World-renowned speakers, the most recent techniques, developments, and the newest updates in Pharmaceutical Analysis are the hallmarks of this conference.

 

Please contact the event manager Marilyn ([email protected] ) below for:
- Multiple participant discounts
- Price quotations or visa invitation letters
- Payment by alternate channels (PayPal, check, Western Union, wire transfers etc)
- Event sponsorships

NO REFUNDS ALLOWED ON REGISTRATIONS
Service fees included in this listing.
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2nd International Conference on Pharmaceutical Analysis & Analytical Chemistry

2nd International Conference on Pharmaceutical Analysis & Analytical Chemistry

About

After the fruitful execution of the International Conference on Pharmaceutical Analysis and Quality Control Strategies, Conference Series with great pride and honour announcing its International Conference on Pharmaceutical Analysis & Analytical Chemistry which is going to held in Chicago, USA during August 02-03, 2020.

Pharmaceutical Analysis 2020 serves as a podium for the interaction between experts in the area of pharmaceutical analysis and analytical chemistry around the world. We cordially invite all the eminent researchers, academicians, students, industry representatives working in these exciting areas.

This Conference is mainly focused on the theme “New paradigms in Pharmaceutical Analytical Techniques”. The conference includes workshops, symposiums, special keynote sessions conducted by eminent and renowned speakers who excel in the field of Pharmaceutical Analysis and Drug Discovery This International Pediatric Conference also encourages the active participation of young student researchers as we are hosting Poster Award Competition and Young research Forum at the conference venue.

Target Audience:

Pharmaceutical Analysis Researchers

Analytical Chemists

Noble Laureates

Directors, Presidents, CEO’s of Organizations/Companies

Pharmaceutical Associations and Societies

Academicians (Professors, Associate & Assistant professors, Deans, Directors)

Graduates and Post graduates

Sessions/Tracks

Track 1: Modern Pharmaceutical Analysis

Generally, Pharmaceutical Analysis alluded to the synthetic examination of medication atoms. Be that as it may, throughout the years, present day pharmaceutical investigation has advanced past this to envelop mix systems, high-throughput innovations, chemo metrics, micro dosing studies, scaling down and nanotechnology. These logical advances are currently being utilized in all phases of medication disclosure and the concentration of this survey will be on how these advances are being utilized inside this procedure. With new, enhanced and advancing innovations, and in addition new applications for existing innovation, the scan for new medications for the aversion and treatment of human maladies proceeds.

Track 2: Chromatography & Separation Techniques

Chromatography strategy for isolating the parts, or solutes, of a blend on the premise of the relative measures of every solute appropriated between a moving liquid streams, called the versatile stage, and a touching stationary stage. The versatile stage might be either a fluid or a gas, while the stationary stage is either a strong or a liquid. Increase in advances in Biotechnology sector augments the production of variety of valuable bio products. Molecules such as therapeutic proteins, enzymes, and other important products require combination of chromatography so as to purify them in purest form. Combination of these novel technologies minimizing the purification steps plays a crucial role for getting maximum purification of the biomolecules.

Track 3: Analytical Method Development and Validation

Analytic method development and validation are persistent and interconnected exercises directed all through the drug development process. The act of validation checks that a given method measures a parameter as planned and sets up the execution furthest reaches of the estimation. Albeit clearly conflicting, approved methods create comes about inside known vulnerabilities. These outcomes are essential to proceeding with drug development, as they characterize the rising learning base supporting the product. The time and exertion that are put into growing logically solid, hearty, and transferrable analytic methods ought to be lined up with the drug development arrange. The assets that are consumed on method validation must be constantly balanced with regulatory requirements and the likelihood for product commercialization.

Track 4: Spectroscopy and its Techniques

Spectroscopy deals with surplus of different techniques that employ electromagnetic radiation on materials in order to measure and interpret data, which is used for elucidating a variety of analytical problems. It includes absorption, emission, or scattering of electromagnetic radiation by atoms or molecules. Types of spectroscopy are IR & NIR, UV/visible, NMR, Atomic Emission Spectroscopy, Fluorescence Spectroscopy etc. Spectroscopic methods are used for Environmental Analysis, Biomedical studies, astronomy. UV-Visible Spectrometer is used for a varied range of applications.

Track 5: Pharmaceutical and Biomedical Analysis

Analytical biochemistry is the study of biochemical components found in a cell or other biological sample. This field uses a broad vary of techniques for separation, identification, quantification and practical characterization of biological molecules like nucleic acids, enzymes, proteins, pigments, carbohydrates and additional. The main ways involved in analytical biochemistry to separate the biological components are qualitative analysis techniques, chromate graphical Techniques, super molecule Estimation & Purification Techniques and medicine Techniques.

Track 6: Mass Spectroscopy: Approaches and Challenges

New mass spectrometry (MS) methods, collectively known as data independent analysis and hyper reaction monitoring. Last decade has witnessed remarkable technological advances in mass spectrometry based proteomics and Biologics. Specific advances include high throughput protein identification by multidimensional chromatography, automated tandem mass spectrometry and sequence data base searching, accurate quantification by the application of stable isotope dilution theory to protein analysis, and the targeted isolation of selected analytes by the use of highly selective chemistries.

Track 7: Bioanalysis

Bioanalysis involves the quantitative measurement of xenobiotics (drugs and their metabolites, and biological molecules in unnatural locations or concentrations) and biotics (macromolecules, proteins, DNA, large molecule drugs, metabolites) in biological systems. In the past two decades, has seen increase in the field of Biopharmaceuticals. Bioanalysis applies to the drugs used for anti-doping testing in sports, illicit purposes and Environmental concerns. The most frequently used techniques are liquid chromatography coupled with tandem mass spectrometry (LC–MS/MS) for micro molecules and enzyme-linked immunosorbent assay (ELISA) for macromolecules.

Track 8: Electro chemical and Thermo analytical techniques

Electrochemical Analysis is a powerful technique that is increasing in utility in the Pharmaceutical Industry due to its high sensitivity, speed of analysis, reduction in solvent and sample consumption, and low operating cost compared to other analytical methods. The modern Electrochemical Analytical techniques are cyclic, linear sweep, differential pulse, square wave and stripping voltammetric techniques. Thermo Analytical techniques are mainly used to detect compound purity, polymorphism, solvation, degradation, and excipient compatibility. It is extensively used in conducting Preformulation studies.

Track 9: Analytical Chemistry

Analytical Chemistry has many applications in Forensic Sciences, environmental analysis, and materials analysis. Analytical Chemistry research is mainly driven by the performance and cost. In these days, great efforts are being put to shrinken the analytical techniques to chip size. In this technology, the most used technique is lab-on-a-chip. The ongoing developments of computer automation and information technologies have broadened the analytical chemistry into a number of new biological fields.

Track 10: Preformulation Studies

Preformulation is considered as critical decision-making tool during both – drug discovery and development phase. Preformulation studies help in assessing the drugability of a molecule. To generate Preformulation data analytical techniques like Spectroscopic, Chromatographic, Thermal methods and some specific detection methods like Capillary electrophoresis are used.

Track 11: Hyphenated Techniques in Analytical chemistry

Hyphenated technique is developed from the coupling of a separation technique and an on-line spectroscopic detection technology. These techniques are mainly broadened their applications in the analysis of natural products.

Track 12: Quality Assurance and Quality Control

Quality assurance is defined as a procedure or set of procedures intended to ensure that a product or service under development meets specified requirements. Quality control (QC) is a procedure or set of procedures intended to ensure that a manufactured product or performed service adheres to a defined set of quality criteria that meets the requirements of the client or customer. The two approaches can be thought of simply as failure detection (QC) and failure prevention (QA). The ISO 9000 family of quality management systems standards is designed to help organizations ensure that they meet the needs of customers and other stakeholders while meeting statutory and regulatory requirements related to a product or service.

Track 13: Pharmaceutical Analysis Errors and Validation

Analytical errors are fundamental before submitting your report and results with the required level of confidence. However, we should have clarity regarding accuracy and precision before we are talking pharmaceutical error. Most of us believe that these terms have the same meaning but the example of arrows striking a target. Any measurement is limited by the precision of the measuring instruments and the technique and the skill of the observer. Where a measurement consists of a single reading on a simple piece of laboratory equipment, for example, a burette or a thermometer, one would expect the quantity of factors adding to vulnerabilities in that estimation to be less than an estimation which is the consequence of a multi-step process comprising of at least two weight estimations, a titration and the utilization of an variety of reagents.

Track 14: GLP and GMP Method Development, Validation and Remediation

Good manufacturing practice is the piece of quality assurance which ensures that things are reliably made and controlled to the quality standard proper to their proposed use and as required by the Marketing Authorization or item particular. GMP is stressed over both generation and quality control, consistency with this standard gives open assurance that the rights, security, and prosperity of trial subjects are ensured; predictable with the rule that have their starting point in the Declaration of Helsinki, and that the clinical information is valid.

Track 15: Biosensors

Biosensor is a device which converts the information regarding the presence of a compound into electro analytical Signal. The biosensor research areas include modern Bio specific analytical techniques. In the recent years, micro fabrication techniques have showed a significant improvement in biosensor systems. The modern methods of the biosensor discoveries range from electrochemical, electromechanical, and fluorescence-­cum-optical-based biosensors and genetically engineered microbes.

Track 16: Pharmaceutical Microbiology

Modern microbiology is unmistakably a branch of biotechnology and incorporates the customary and nucleic corrosive aspects. Pharmaceutical microbiology is the connected branch of microbiology which enables drug specialists to make pharmaceuticals from microorganisms either straightforwardly or with the utilization of some item delivered by them. Different parts of pharmaceutical microbiology incorporate innovative work for assembling of different hostile to tumours, against microbial specialists.

Track 17: Forensic Analysis

Multiply hyphenated techniques, such as gas chromatography/ mass spectrometry with retention time locking (GC/MS/RTL), liquid chromatography/time-of-flight mass spectrometry (LC/ MS/TOF), micro fluidic-based capillary electrophoretic analysis of mitochondrial DNA (mtDNA), and laser ablation inductively coupled plasma mass spectrometry (LA/ICP/MS), are able to uncover forensically germane information by providing unprecedented levels of analytical selectivity and sensitivity

Track 18: Radio Analytical Techniques

Radio analytical Techniques focuses on analysis of sample for their radionuclide content. The Radio analytical Chemistry Capability (RACC) combines radioanalytical chemistry and medium level gamma-ray spectrometry. It has wide applications in the field of forensics, atmospheric sciences, health protection, archeology, and engineering.

Please contact the event manager Marilyn (marilyn.b.turner(at)nyeventslist.com ) below for:
- Multiple participant discounts
- Price quotations or visa invitation letters
- Payment by alternate channels (PayPal, check, Western Union, wire transfers etc)
- Event sponsorship

NO REFUNDS ALLOWED ON REGISTRATIONS
Prices may go up any time. Service fees included in pricing.
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23rd International Conference on Advanced Materials & Nanotechnology (CSE)

23rd International Conference on Advanced Materials & Nanotechnology


About Conference
ConferenceSeries LLC Ltd is proud to announce the 23rd International Conference on Advanced Materials and Nanotechnology, which is to be held during August 19-20, 2020 at Tokyo, Japan.

On this great gathering, Organizing Committee invites participants from all over the globe to take part in this annual conference with the theme “Exploring the Possibilities in the Field of Advanced Materials and Nanotechnology”. Advanced Materials 2020 aims at sharing new ideas and new technologies amongst the professionals, industrialists and students from research areas of Advanced Materials and Nanotechnology to share their recent innovations and applications and indulge in interactive discussions and technical sessions at the event. The Conference will also have a space for companies and/or institutions to present their services, products, innovations and research results. 

Advanced Materials and Nanotechnology involves the tracks like Advanced Materials and Functional Devices, Engineering Materials, Composite Materials, Magnetism & Multiferroism, Optical materials and plasmonics, Energy and Harvesting Materials, Nanotechnology-Basics to applications, Nanopore science, Nanomedicine, Bio Nanotechnologies, Carbon nanostructures and graphene, Spintronics, Nanoparticle synthesis and applications.

Importance and Scope:

Advanced Materials plays a vital role in our lives because of its uniqueness in properties and extended application in various industries. These are the basis of modern science and technology. Advanced Materials are at the heart of many technological developments that touch our lives and find applications such as electronic materials for communication and information technology, biomaterials for better health care, sensors for intelligent environment, energy materials for renewable energy and environment, light alloys for better transportation, materials for strategic applications and more.

Nanotechnology is science, engineering, and technology conducted at the nanoscale, which is about 1 to 100 nanometers. Nanotechnology is the study of application of extremely small things and can be used across all the other science fields, such as chemistry, biology, physics, materials science, and engineering. Today's scientists and engineers are finding a wide variety of ways to deliberately make materials at the nanoscale to take advantage of their enhanced properties such as higher strength, lighter weight, increased control of light spectrum, and greater chemical reactivity than their larger-scale counterparts

Why to attend???

23rd International Conference on Advanced Materials and Nano-Technology professionals providing a premier technical forum for reporting and learning about the latest new generation technologies developed during the course of time along with discussing their applications. Events include hot topics presentations from all over the world and professional networking with industries, leading working groups and panels.

Meet Your Objective Business sector With individuals from and around the globe concentrated on finding out about Polymer science and Engineering, this is the best chance to achieve the biggest collection of members from everywhere throughout the World. Conduct shows, disperse data, meet with current, make a sprinkle with another product offering, and get name acknowledgment at this occasion. Widely acclaimed speakers, the latest methods, strategies, and the most up to date overhauls in Polymer science and Engineering are signs of this meeting.

Target Audience:

Scientists.
Professors.
Research Scholars and students
Nanotechnology Companies
Nanotechnology Associations
Advanced Materials and Nanotechnology Engineers

Sessions/Tracks

Track 1: Advanced Materials and Functional Devices

This is The Creation of Advanced Materials at The Molecular or Nuclear Measure for the reason for propelling innovation, growing further effective items, making novel assembling advances, or enhancing the human learning. The capacity to rapidly and dependably set out numerous conductive layers with ultrafine determination has prompted the scaling down and minimal effort of most microelectronic parts. Practical Devices has set up itself as a pioneer in the HVAC, Building Controls, Energy Management, Energy Savings, Lighting Controls, and Wireless enterprises.

Materials engineering, materials science and engineering, engineering materials, material science, advanced materials in civil engineering, advances in materials science and engineering, advanced materials in automotive engineering, Electronic materials, chemical materials 

Track 2: Engineering Materials

The Materials used for Manufacturing of engineering products are termed engineering materials. These engineering materials are the backbone of all engineering products. The design, manufacturing, commercialization and performance of any engineering products are basically depends on the material being used for that product.

advanced engineering materials, engineered materials solutions, huber engineered materials, material engineer, engineered materials solutions, callister materials science and engineering, bioengineering and tissue engineering, Polymer Science and Engineering, Metals and Metallurgy, Powder metallurgy, lasers

Track 3: Composite Materials

A materials structure made out of no less than two physically one of a kind stages whose mix produces add up to properties that are not the same as those of its constituents. Composites can be incredibly strong and solidified, yet light in weight, so extents of value to weight and solidness to weight are a couple of conditions more essential than steel or aluminum.

composite materials, composite decking material, jps composite materials, aluminum composite material, composite roofing material, composite building materials, composite fencing materials, mechanics of composite materials, advanced composite materials, plastic, plastic sheets, plastic surgery, plastic welding, plastic containers, plastic recycling, ceramic, ceramics, polymer, polymer clay, polymer 80, carbohydrate polymers, organic polymer ark

Track 4: Magnetism & Multiferroism

Attraction is one part of the joined electromagnetic drive. It alludes to physical wonders emerging from the compel brought about by magnets, protests that create fields that draw in or repulse different items. The blend of a few ferric arranges in a similar material, instituted under the term of Multiferroism as of late gotten a great deal of consideration.

electromagnetic field, magnetic particles, Magnetism, electronic magnetic pulse, rare earth magnets, magnetic field, neodymium magnets, magnetic eyelashes, magnet toys, car magnets, magnetic phone charger

Track 5: Optical Materials and Plasmonics

The Diligence of Optical Materials is to give a technique for correspondence and development trade among researchers who are careful in materials for potential contraption applications. Plasmonics is the examination of the joint effort between electromagnetic field and free electrons in a metal.

advanced optical materials, optical materials, fiber optic material, fiber optic cable raw materials, electronic magnetic and optical materials, optical fiber cladding material

Track 6: Energy and Harvesting Materials

The examination of imperativeness gathering materials is experiencing remarkable improvement and pulling in colossal premium. Abusing starting late picked up dreams into the real instruments and benchmarks of photosynthesis, it is by and by possible to mold absolutely new and specific sub-nuclear materials and devise fake photosystems and applications far remote from routine sun based cell development.

energy harvesting materials, power harvesting using piezoelectric materials, roof material for rainwater harvesting, piezoelectric materials for energy harvesting, energy harvesting from piezoelectric materials, solar energy

Track 7: Nanotechnology-Basics to Applications

Nanotechnology is the coordinated effort of the physical science, chemistry, biology, computer and material sciences incorporated with designing entering the nanoscale. This implies science and building concentrated on making the particles things and gadgets at the nuclear and atomic scale. The Study of the Controlling of Matter on an atomic and sub-nuclear scale. Generally Nanotechnology Deals with Structures Sized between 1 to 100 Nanometre in no short of what one Dimension, and incorporates making or changing materials or devices inside that size.

nano technology, nano crystal technology, nano technologies

Track 8: Nano Materials

Nanomaterials are foundations of nanoscience and nanotechnology. Nanostructure science and advancement is a sweeping and interdisciplinary space of imaginative work improvement that has been winding up brutally worldwide in the recent years. It has the potential for changing the courses in which materials and things are made and the range and nature of functionalities that can be gotten to.nano materials, nano one materials, nano structured materials, properties of nano material, nanoscale, nanoscale engineering

Track 9: Nano Structures

Nanostructured Materials (NsM) are Advancedmaterials with a microstructure the trademark length size of which is on the request of a couple (routinely 1– 10) nanometers. NsM might be in or far from thermodynamic concordance. Nanostructured Materials joined by supramolecular science are occasions of Nanostructured Materials in thermodynamic assention. Nanostructured Materials containing nanometer-sized crystallites (e.g. of Au or NaCl) with various crystallographic introductions or possibly fabricated indications are far from thermodynamic friendliness.

Track 10: Properties of Nano Materials

Nanoparticles are striking because of their tremendous surface area and this principles the duties made by the little heave of the material. Zinc oxide particles have been found to have better UV blocking properties contemplated than its mass substitute.

Track 11: Carbon Nanostructures and Graphene

Carbon is immovably connected with about all that we oversee in a general timetable. Due to its remarkable properties, for instance, high robustness at normal conditions, differing hybridizations, strong covalent bond game plan and straightforward of blends advancement, carbon has been a state of consistent excitement for a couple of districts. A nanostructure is a structure of fair size among minute and nuclear structures. Nano structural detail is microstructure at nanoscale.

Graphene is an allotrope of carbon as a two-dimensional, atomic scale, hexagonal cross segment in which one particle shapes each vertex. It is the basic helper segment of various allotropes, including graphite, charcoal, carbon nanotubes and fullerenes. It can moreover be considered as an uncertainly significant sweet-noticing iota, an authoritative occurrence of the gathering of level polycyclic fragrant hydrocarbons.

carbon fiber, carbon fiber wrap, carbon fiber sheets, carbon fiber tube, carbon fiber wheels, carbon fiber bike, carbon fiber rims, Graphene, graphene battery, graphene aerogel, graphene oxide, graphene supercapacitor, graphene sheet, grapheme, graphene armor, graphene applications

Track 12: Spintronics

Spintronics is the usage of a basic property of particles known as turn for information planning. From various perspectives, spintronics is undifferentiated from contraptions, which rather uses the electrical charge on an electron. Passing on information in both the charge and turn of an electron perhaps offers contraptions with more imperative contrasts of handiness.

Spintronics, spintron centrifuge, spintronic transistor, spintronics applications, spintronics graphene, spintronic materials, spintronic device, semiconductor spintronics

Track 13: Nanoparticle Synthesis and Applications

Nanoparticle blend alludes to techniques for making nanoparticles. Nanoparticles can be gotten from

Bigger atoms, or blended by 'base up' techniques that, for instance, nucleate and develop particles from fine sub-atomic appropriations in fluid or vapour stage. Blend can likewise incorporate functionalization by conjugation to bioactive particles.

Nanoparticles have one estimation that measures 100 nanometres or less. The properties of various conventional materials change when moulded from nanoparticles. This is routinely in light of the way that nanoparticles have a more important surface range per weight than greater particles which make them be more receptive to some unique iotas.

AGENDA 2020

----------------------------------
2020 Upcoming Soon
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DAY-1
September 04, 2020
Meeting Hall: London B
08:00-8:30 Registrations
Opening Ceremony 08:30-08:55
Keynote Forum
08:55-09:00 Introduction
09:00-09:40 Title: Hybrid conversion Solar System (HYCSOS)
Dieter M Gruen, Dimerond Technologies, USA
09:40-10:20
Title: Semiconductors and semiconductor-ionic heterostructure composites for next generation
energy conversion technology
Bin Zhu, Hubei University, China
SPECIAL SESSION
10:20-11:20 Title: On the way to physically correct indentation analyses
Gerd Kaupp, University of Oldenburg, Germany
Group Photo, Networking & Refreshments 11:20-11:40 @ Europa Foyer
Sessions: Advanced Materials Engineering | Emerging Areas of Materials Science | Environmental and Green
Materials | Carbon Based Materials | Advanced Bio-Materials and Bio-devices | Energy Materials and Harvesting
Chair: Roger Amade, Universitat de Barcelona, Spain
Chair: Toshihiro Miyata, Kanazawa Institute of Technology, Japan
Introduction
11:40-12:00 Title: Adsorbent materials for desulfurization processes under supercritical water conditions
Florentina Maxim, Paul Scherrer Institut, Swizerland
12:00-12:20
Title: Realization of conductive aluminum nitride epitaxial layer on silicon substrate by forming
spontaneous nano size via-holes
Noriko Kurose, Ritsumeikan University, Japan
12:20-12:40
Title: A new laser induced local material engineering to convert from n-type to p-type nitride
semiconductor to fabricate high power vertical AlGaN/GaN devices on Si substrate
Yoshinobu Aoyagi, Ritsumeikan University, Japan
12:40-13:00
Title: Restoration of perovskite phase in the top layer of thin BTO film by plasma treatment and
annealing
Ankita Ghatak, S.N. Bose National Centre For Basic Sciences, India
Page 3
conferenceseries.com
13:00-13:20 Title: Hybrid perovskite halide for detection of environmental pollutant in atmosphere
Barnali Ghosh (Saha), S.N. Bose National Centre For Basic Sciences, India
Lunch Break 13:20-14:00 @ La Place AB
14:00-14:20 Title: Comparative analysis on monolithic DeNOx catalysts
Giovanni Perillo, Wessex Institute of Technology, UK
14:20:14:40 Title: Growth and electrochemical characterization of graphene nano walls and carbon nanotubes
Roger Amade, Universitat de Barcelona, Spain
14:40-15:00 Title: Fine-controlled sub-nano metal particles in a dendrimer reactor
Kimihisa Yamamoto, Tokyo Institute of Technology, Japan
15:00-15:20 Title: Thermoelectricity enhanced catalysis
Tiva Sharifi, Rice University, USA
15:20-15:40
Title: P-type Cu2O-based heterojunction solar cells fabricated with n-type ZnO thin film prepared
by electrochemical deposition method
Toshihiro Miyata, Kanazawa Institute of Technology, Japan
15:40-16:00
Title: Growth control of vertical nano graphene network in plasma enhanced chemical vapor
deposition and its emerging applications
Keigo Takeda, Meijo University, Japan
16:00-16:20 Title: In silico study of the self-assembly and gelation of sugar derivatives
Dafna Knani, ORT Braude College, Israel
Networking & Refreshments 16:20-16:40 @ Europa Foyer
16:40-17:00 Title: Design and development of nanomaterials using induction plasma system and its application
Vignesh Nagarajan, Matrix Nano, India
YRF
YRF Judge: Gerd Kaupp, University of Oldenburg, Germany
17:00-17:15 Title: Development of functionalized coating by sol-gel process on aluminium alloy
Clément Genet, Université de Toulouse, France
17:15-17:30 Title: Developing super hydrophobic copper/graphene nano-platelets coatings by plasma spraying
Tahmineh Forati, Concordia University, Canada
17:30-17:45
Title: Novel carbon nanomaterials coated with CuO particles via electroless plating for
nonothermite applications
Amir Elsaidy, Military Technical College, Egypt
17:45-18:00 Title: Functionalized track-etched PVDF membrane electrodes for heavy metal analysis in water
Uliana Pinaeva, Ecole Polytechnique, France
Panel Discussion

DAY-2
September 05, 2020
Meeting Hall: London B
Keynote Forum
09:00-09:40 Title: Driving flexible electronics by hybrid materials
Rodrigo Martins, New University of Lisbon, Portugal
09:40-10:20 Title: Switching iron-based superconductivity with spin current
Jhinhwan Lee, Korea Advanced Institute of Science and Technology, South Korea
Sessions: Advanced Functional Materials | Polymers Scicence and Engineering | Advanced Optical Materials |
Advancement in Nanomaterials Science and Nanotechnology | Coating and Surface Engineering
Chair: Dieter M Gruen, Dimerond Technologies, USA
Chair: Yutaka Oyama, Tohoku University, Japan
Introduction
10:20-10:40 Title: Relation between internal friction and fatigue
Wolfgang Gräfe, Private Scholar, Germany
10:40-11:00
Title: Improvement of CFRP electrical conductivity by applying nano enabled products containing
carbon nanotubes
Anna Boczkowska, Warsaw University of Technology, Poland
11:00-11:20
Title: Boron carbide-based ceramics for thermostructural application: Sintering by SPS and
mechanical performances
Alexandre Maître, University of Limoges, France
Networking & Refreshments 11:20-11:40 @ Europa Foyer
11:40-12:00
Title: Synthesis of 2D layered semiconductor GaSe for the application of Terahertz non-destructive
inspection
Yutaka Oyama, Tohoku University, Japan
12:00-12:20 Title: Solution deposition of Cu doped Co3O4 ffor electrooxidation of glucose
Mahabubur Chowdhury, Cape Peninsula University of Technology, South Africa
12:20-12:40
Title: Cu metal/Mn phthalocyanine organic sprinter faces atop Co with high spin polarization at
room temperature
Wolfgang Weber, Université de Strasbourg, France
12:40-13:00 Title: Producing of aluminium matrix composite wire
Janos Dobranszky, Budapest University of Technology and Economics, Hungary
13:00-13:20 Title: Chitosan asiaticoside nanoparticles synthesized from Centella asiatica for glioma therapy
V Gayathri, Jawaharlal Nehru Tropical Botanic Garden and Research Institute, India
Lunch Break 13:20-14:00 @ La Place AB
14:00-14:20 Title: Investigation on weldability behavior of chromium-free nickel filler with stainless steel AISI-304
Nataraj J.R, R.V.College Of Engineering, India
14:20-14:40
Title: Multiferroic Properties and Structural Characterizations in Mn and Cr Doped 0.9BiFeO3-
0.1BaTiO3 Compositions
Ricardo A. M Gotardo, Technological Federal University of Paraná, Brazil
14:40-15:00
Title: Synthesis of Pt-WO3@W/GNs as a bifunctional electro-photo catalyst for catalyzing
methanol oxidation and oxygen reduction reaction
Shen Lin, Fujian Normal University, China
15:00-15:20 Title: Low-cost printable hybrid hetero structures for energy harvesting and lighting
Sylvain G. Cloutier, Ecole de Technologie Superieure, Canada
15:20-15:40 Title: New generation of Colorcoat Prisma®
Anna Lewandowska, Tata Steel UK Limited, United Kingdom
Networking & Refreshments 15:40-16:00 @ Europa Foyer
YRF
YRF Judge: Gerd Kaupp, University of Oldenburg, Germany
16:00-16:15 Title: FEM analysis for burring process of large diameter SUS304 tube
Junshi Ichikawa, Gunma University, Japan
16:15-16:30 Title: Horizontal twin roll casting of aluminum alloy A7075
Yuta Kashitani, Gunma University, Japan
16:30-16:45 Title: Cold plastic forming of ABS plastic pipe: ABS plastic pipe
Kentaro Tsunoda, Gunma University, Japan
16:45-17:00
Title: Engineering protein interfaces yields ferritin disassembly and reassembly under benign
experimental conditions
Hai Chen, China Agricultural University, China
17:00-17:15 Title: Dynamic analyses of damping alloy sleeves for boring
Yuto Horigome, Gunma University, Japan
17:15-17:30 Title: Infrared spectra of aluminum fluorocarbon polymer compositions to thermal signature of jet engine
Amir Elsaidy, Military Technical College, Egypt
17:30-17:45 Title: Thermoelectric properties of ZnO-based ceramics prepared by spark plasma sintering technique
Radingoana Precious Manti, Université de Toulouse, France
Poster Presentations 17:45-18:30
Poster Judge: Anna Boczkowska, Warsaw University of Technology, Poland
AM-01
Title: Fabrication of micro/nano-crystals of organic Dirac fermion system: nano-scale electro
crystallization
Takako Konoike, National Institute for Materials Science, Japan
AM-02 Title: Synthesis by hydrogen reduction and characterization of CuNiCo with nanoparticles content
Eduardo Brocchi, Pontifical Catholic University of Rio de Janeiro, Brazil
AM-03 Title: One-pot synthesis of hybrid nano particles for catalytic applications
Heeyeon Kim, Korea Institute of Energy Research, South Korea
AM-04 Title: Chitosan delaying human fibroblast senescence through down regulation of TGF-β signaling pathway
Tai-Horng Young, National Taiwan University, Taiwan
AM-05 Title: Ag+ ion emission from a sharp tip of Ag+ ion conducting glass and Schottky-model analysis
Yusuke Daiko, Nagoya Institute of Technology, Japan
AM-06 Title: Effect of electrolyte aging on the morphology and mechanical properties of anodic titanium dioxide
Junzhe Dong, The University of Auckland, New Zealand
AM-07 Title: Magnetic carbon nano materials as matrices for the immobilization of cellulolytic enzymes
Athena Papadopoulou, University of Ioannina, Greece
AM-08 Title: Surface texturing with slanted silicon nano pillars to reduce its optical reflectivity
Jun-hyun Kim, Ajou University, South Korea
AM-09 Title: Simulation and development of counter weight casting
Koushik Kosanam, R.V.College Of Engineering, India
AM-10 Title: Study of fragmentation and ultrasonic flow impacts of several metal-based alloys
Abdulrahman Sumayli, University of Hull, UK
AM-11 Title: Effect of epoxidized cardanol on poly(vinyl chloride) as secondary plasticizer
Jie Chen, Chinese Academy of Forestry, China
AM-12
Title: Eu2+/Eu3+-activated nitride based red phosphors with narrow emission band for white light
emitting diodes
Jianyan Ding, Lanzhou University, China
AM-13
Title: K4CaGe3O9:Mn2+, Yb3+: a novel orange-emitting long persistent luminescence phosphor
with special nano structure
Xufeng Zhou, Lanzhou University, China
AM-14
Title: A composite of MnO2 coated with graphene by galvanostatic electrodeposition and its
highly active and stable catalysis for oxygen reduction reaction
Xiaofeng Zhang, Fujian Normal University, China
AM-15 Title: Ni-based nanowire co-catalysts integrated with a Si photoanode for efficient water oxidation
Meshal S Aljohani, King Abdulaziz City for Science and Technology, Saudi Arabia
AM-16
Title: Facile synthesis of laminated porous WS2/C composite and its electrocatalysis for oxygen
reduction reaction
Zhongshui Li, Fujian Normal University, China
AM-17 Title: Graphene oxide-copper hybrid nanoflowers for the efficient immobilization of enzymes
Athena Papadopoulou, University of Ioannina, Greece
AM-18 Title: Advances in 3D printing in biomaterials for orthopaedic applications
Daniel Li, Northwestern University, USA
Panel Discussion

DAY-3
September 06, 2020
Networking & lunch 12:30-14:00 @ La Place AB
Awards & Closing Ceremony

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