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.
Pharmaceutical Analysis Researchers
Directors, Presidents, CEO’s of Organizations/Companies
Pharmaceutical Associations and Societies
Academicians (Professors, Associate & Assistant professors, Deans, Directors)
Graduates and Post graduates
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.
Conference Series. - New York Events List