BEGIN:VCALENDAR VERSION:2.0 PRODID:icalendar-ruby CALSCALE:GREGORIAN BEGIN:VEVENT DTSTAMP:20240329T101559Z UID:3330d3b9-262b-4e16-94c6-41bf7b6e4bae DTSTART:20240803T000000 DTEND:20240804T000000 CLASS:PRIVATE DESCRIPTION:
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\nPhar
maceutical Analysis 2020
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\n\nAfter the fr uitful execution of the International Conference on Pharmaceutical Analysi s 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.
\n\nPharmaceutical Analysis 2020 serves as a p odium for the interaction between experts in the area of pharmaceutical an alysis and analytical chemistry around the world. We cordially invite all the eminent researchers\, academicians\, students\, industry representativ es working in these exciting areas.
\n\nThis Conference is mainly fo cused on the theme &ldquo\;New paradigms in Pharmaceutical Analytical Tech niques&rdquo\;. The conference includes workshops\, symposiums\, special k eynote sessions conducted by eminent and renowned speakers who excel in th e field of Pharmaceutical Analysis and Drug Discovery This International P ediatric Conference also encourages the active participation of young stud ent researchers as we are hosting Poster Award Competition and Young resea rch Forum at the conference venue.
\n\nTarget Audience:
\n\nPharmaceutical Analysis Researchers
\n \nAnalytical Chemists
\nNoble Laureates
\nDirectors\, Presidents\, CEO&rsquo\;s of Organiza tions/Companies
\nPharmaceutical Associations and So cieties
\nAcademicians (Professors\, Associate &\ ; Assistant professors\, Deans\, Directors)
\nGradua tes and Post graduates
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\n\nSessions/Tracks
\n\nTrack 1: Modern Pharmaceutical Analysis
\n\nGenerally\, Pharmaceutical Analysis alluded to the synthetic examination of medication atoms. Be that as it may\, throug hout the years\, present day pharmaceutical investigation has advanced pas t this to envelop mix systems\, high-throughput innovations\, chemo metric s\, micro dosing studies\, scaling down and nanotechnology. These logical advances are currently being utilized in all phases of medication disclosu re and the concentration of this survey will be on how these advances are being utilized inside this procedure. With new\, enhanced and advancing in novations\, and in addition new applications for existing innovation\, the scan for new medications for the aversion and treatment of human maladies proceeds.
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\n\nTrack 2: Chromatography &am p\; Separation Techniques
\n\nChromatography strategy for i solating the parts\, or solutes\, of a blend on the premise of the relativ e measures of every solute appropriated between a moving liquid streams\, called the versatile stage\, and a touching stationary stage. The versatil e stage might be either a fluid or a gas\, while the stationary stage is e ither a strong or a liquid. Increase in advances in Biotechnology sector a ugments 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. Combina tion of these novel technologies minimizing the purification steps plays a crucial role for getting maximum purification of the biomolecules.
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\n\nTrack 3: Analytical Method Development and V alidation
\n\nAnalytic method development and validation ar e persistent and interconnected exercises directed all through the drug de velopment process. The act of validation checks that a given method measur es a parameter as planned and sets up the execution furthest reaches of th e estimation. Albeit clearly conflicting\, approved methods create comes a bout inside known vulnerabilities. These outcomes are essential to proceed ing with drug development\, as they characterize the rising learning base supporting the product. The time and exertion that are put into growing lo gically solid\, hearty\, and transferrable analytic methods ought to be li ned 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.
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\n \nTrack 4: Spectroscopy and its Techniques
\n\nS pectroscopy deals with surplus of different techniques that employ electro magnetic radiation on materials in order to measure and interpret data\, w hich is used for elucidating a variety of analytical problems. It includes absorption\, emission\, or scattering of electromagnetic radiation by ato ms or molecules. Types of spectroscopy are IR &\; NIR\, UV/visible\, NM R\, Atomic Emission Spectroscopy\, Fluorescence Spectroscopy etc. Spectros copic methods are used for Environmental Analysis\, Biomedical studies\, a stronomy. UV-Visible Spectrometer is used for a varied range of applicatio ns.
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\n\nTrack 5: Pharmaceutical and Biomed ical Analysis
\n\nAnalytical biochemistry is the study of b iochemical components found in a cell or other biological sample. This fie ld uses a broad vary of techniques for separation\, identification\, quant ification and practical characterization of biological molecules like nucl eic acids\, enzymes\, proteins\, pigments\, carbohydrates and additional. The main ways involved in analytical biochemistry to separate the biologic al components are qualitative analysis techniques\, chromate graphical Tec hniques\, super molecule Estimation &\; Purification Techniques and med icine Techniques.
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\n\nTrack 6: Mass Spectr oscopy: Approaches and Challenges
\n\nNew mass spectrometry (MS) methods\, collectively known as data independent analysis and hyper reaction monitoring. Last decade has witnessed remarkable technological ad vances in mass spectrometry based proteomics and Biologics. Specific advan ces include high throughput protein identification by multidimensional chr omatography\, automated tandem mass spectrometry and sequence data base se arching\, accurate quantification by the application of stable isotope dil ution theory to protein analysis\, and the targeted isolation of selected analytes by the use of highly selective chemistries.
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\n\nTrack 7: Bioanalysis
\n\nBioanalysis involve s 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\, metaboli tes) in biological systems. In the past two decades\, has seen increase in the field of Biopharmaceuticals. Bioanalysis applies to the drugs used fo r anti-doping testing in sports\, illicit purposes and Environmental conce rns. The most frequently used techniques are liquid chromatography coupled with tandem mass spectrometry (LC&ndash\;MS/MS) for micro molecules and e nzyme-linked immunosorbent assay (ELISA) for macromolecules.
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\n\nTrack 8: Electro chemical and Thermo analytical tec hniques
\n\nElectrochemical Analysis is a powerful techniqu e that is increasing in utility in the Pharmaceutical Industry due to its high sensitivity\, speed of analysis\, reduction in solvent and sample con sumption\, and low operating cost compared to other analytical methods. Th e modern Electrochemical Analytical techniques are cyclic\, linear sweep\, differential pulse\, square wave and stripping voltammetric techniques. T hermo Analytical techniques are mainly used to detect compound purity\, po lymorphism\, solvation\, degradation\, and excipient compatibility. It is extensively used in conducting Preformulation studies.
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Track 9: Analytical Chemistry
\n\nAnalytic al Chemistry has many applications in Forensic Sciences\, environmental an alysis\, and materials analysis. Analytical Chemistry research is mainly d riven by the performance and cost. In these days\, great efforts are being put to shrinken the analytical techniques to chip size. In this technolog y\, the most used technique is lab-on-a-chip. The ongoing developments of computer automation and information technologies have broadened the analyt ical chemistry into a number of new biological fields.
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Track 10: Preformulation Studies
\n\nPrefo rmulation is considered as critical decision-making tool during both &ndas h\; drug discovery and development phase. Preformulation studies help in a ssessing the drugability of a molecule. To generate Preformulation data an alytical techniques like Spectroscopic\, Chromatographic\, Thermal methods and some specific detection methods like Capillary electrophoresis are us ed.
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\n\nTrack 11: Hyphenated Techniques in Analytical chemistry
\n\nHyphenated technique is developed from the coupling of a separation technique and an on-line spectroscopic detection technology. These techniques are mainly broadened their applicat ions in the analysis of natural products.
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\n\nQua lity assurance is defined as a procedure or set of procedures intended to ensure that a product or service under development meets specified require ments. Quality control (QC) is a procedure or set of procedures intended t o ensure that a manufactured product or performed service adheres to a def ined 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 manageme nt systems standards is designed to help organizations ensure that they me et the needs of customers and other stakeholders while meeting statutory a nd regulatory requirements related to a product or service.
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\n\nTrack 13: Pharmaceutical Analysis Errors and Validat ion
\n\nAnalytical 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 talk ing pharmaceutical error. Most of us believe that these terms have the sam e meaning but the example of arrows striking a target. Any measurement is limited by the precision of the measuring instruments and the technique an d the skill of the observer. Where a measurement consists of a single read ing on a simple piece of laboratory equipment\, for example\, a burette or a thermometer\, one would expect the quantity of factors adding to vulner abilities in that estimation to be less than an estimation which is the co nsequence of a multi-step process comprising of at least two weight estima tions\, a titration and the utilization of an variety of reagents.
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\n\nTrack 14: GLP and GMP Method Development\, Va lidation and Remediation
\n\nGood manufacturing practice is the piece of quality assurance which ensures that things are reliably mad e and controlled to the quality standard proper to their proposed use and as required by the Marketing Authorization or item particular. GMP is stre ssed over both generation and quality control\, consistency with this stan dard gives open assurance that the rights\, security\, and prosperity of t rial subjects are ensured\; predictable with the rule that have their star ting point in the Declaration of Helsinki\, and that the clinical informat ion is valid.
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\n\nTrack 15: Biosensors
\n\nBiosensor is a device which converts the information regar ding the presence of a compound into electro analytical Signal. The biosen sor research areas include modern Bio specific analytical techniques. In t he recent years\, micro fabrication techniques have showed a significant i mprovement in biosensor systems. The modern methods of the biosensor disco veries range from electrochemical\, electromechanical\, and fluorescence-& shy\;cum-optical-based biosensors and genetically engineered microbes.
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\n\nTrack 16: Pharmaceutical Microbiology
\n\nModern microbiology is unmistakably a branch of biotechnol ogy and incorporates the customary and nucleic corrosive aspects. Pharmace utical microbiology is the connected branch of microbiology which enables drug specialists to make pharmaceuticals from microorganisms either straig htforwardly or with the utilization of some item delivered by them. Differ ent parts of pharmaceutical microbiology incorporate innovative work for a ssembling of different hostile to tumours\, against microbial specialists.
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\n\nTrack 17: Forensic Analysis< /p>\n\n
Multiply hyphenated techniques\, such as gas chromatography/ mas s spectrometry with retention time locking (GC/MS/RTL)\, liquid chromatogr aphy/time-of-flight mass spectrometry (LC/ MS/TOF)\, micro fluidic-based c apillary electrophoretic analysis of mitochondrial DNA (mtDNA)\, and laser ablation inductively coupled plasma mass spectrometry (LA/ICP/MS)\, are a ble to uncover forensically germane information by providing unprecedented levels of analytical selectivity and sensitivity
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\n\ nTrack 18: Radio Analytical Techniques
\n\nRadio analytical Techniques focuses on analysis of sample for their radionuclid e content. The Radio analytical Chemistry Capability (RACC) combines radio analytical chemistry and medium level gamma-ray spectrometry. It has wide applications in the field of forensics\, atmospheric sciences\, health pro tection\, archeology\, and engineering
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\n\nWhy to Attend
\n\nPharmaceutical Analysis will provide you a great opportunity to meet with like-minded people and industry peers. T his is the best place to present your research in front of the global audi ence coming from the different countries. World-renowned speakers\, the mo st recent techniques\, developments\, and the newest updates in Pharmaceut ical Analysis are the hallmarks of this conference.
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\ n\nPlease contact the event manager Marilyn (marilyn.b.turner@nyeventsl
ist.com ) below for:
\n- Multiple participant discounts
\n- Pric
e quotations or visa invitation letters
\n- Payment by alternate chan
nels (PayPal\, check\, Western Union\, wire transfers etc)
\n- Event
sponsorships
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\nNO REFUNDS ALLOWED ON REGISTRATIONS
\nSer
vice fees included in this listing.
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ents List
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MYL181127UPR
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\nReference:
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\nhttps://www.eventbr
ite.com/e/conference-on-pharmaceutical-analysis-analytical-chemistry-cse-a
s-tickets-50210944286