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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MYL180913CEV

Reference:

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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

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

Kallol K. Ghosh

Professor
Pt. Ravishankar Shukla University, Raipur , India
India

 

Edward Lee Ruff

Professor
York University
USA

 

Yuichi Shimazaki

Professor
Ibaraki University
Japan

 

Maged Henary

Professor
Georgia State University 
USA

 

Mahesh N. Sanzgiri,

Professor
St. Xavier’s College
India

 

Romano VA Orru

Professor
VU University
Netherland

 

Majid M Heravi

Professor
Alzahra University
Iran

 

Waldemar Adam

Professor Emeritus
University of Puerto Rico
Puerto Rico

 

Jun Yin

Associate Professor
Georgia State University
United States

 

P. Gregory Van Patten

Department Chair
Middle Tennessee State University
United States

 

Xin-Tao Wu

Professor
Chinese Academy of Sciences
China

 

Yong-Li Zhong

Principal Scientist
Merck & Co., Inc.
USA

 

Saad Alotaibi

Dean of Turabah Abdullah university
Taif University
Kingdom of Saudi Arabia

 

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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Reference:

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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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http://www.NyEventsList.com
http://www.BostonEventsList.com
http://www.SFBayEventsList.com
-----------------------------------------------------------------

MYL180913CEV MYL181127UPR

Reference:

https://www.eventbrite.com/e/conference-on-pharmaceutical-analysis-analytical-chemistry-cse-as-tickets-50210944286

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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