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Pharmaceutical Analysis 2019

About Conference


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 and Drug Discovery which is going to held in San Diego, USA during June 28-29, 2019.

Pharmaceutical Analysis 2019 serves as a podium for the interaction between experts in the area of pharmaceutical analysis, drug discovery, nanotechnology and regulatory departments involved in drug discovery 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 “Comprehensive Drug Research by Fostering Innovative 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

Drug Discovery scientists

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.

Recommended: WORLD PHARMA CONGRESS 2018 | PHARMA FORMULATIONS 2018 | PHARMA RESEARCH 2019 | PHARMA NANO 2019

Related Conferences: 11th World Congress on Pharmaceutical Sciences, September 28-29, 2018, Montreal, Canada, 15th International Conference on Pharmaceutical Formulations & Drug Delivery, September 17-18, 2018, Philadelphia, Pennsylvania, USA, 2nd International Conference & B2B on Pharma Research and Development, April 26-27, 2019, Houston, USA, 2nd International Conference and Exhibition on Pharmaceutical Nanotechnology and Nanomedicine, March 20-21, 2019, New York , USA, 9th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR, March 20-21, 2019 Houston, USA, Annual Bio analytical Conference, July 9-12, 2018, Madison, Wisconsin, USA, AAPS Pharma Sci360, November 4-7, 2018, Washington,USA

Related Societies USA: American Association of Pharmaceutical Scientists, Association of Clinical Research Organizations, Pharmaceutical Research and Manufacturers of America

Related Societies Europe: The European Federation For Pharmaceutical Sciences, Pharmaceutical Group of the European Union, Association of the British Pharmaceutical Industry

Related Societies Asia Pacific: Federation of Asian Pharmaceutical Associations, Pharmaceutical Research and Manufacturers Association, International Pharmaceutical Manufacturers Group

Track 2: Drug Discovery & Development

It is the process to discover a new drug and bringing a drug to the market once a lead compound has been identified through the process of drug discovery. It includes pre-clinical research on microorganisms and animals, filing for regulatory status, such as via the United States Food and Drug Administration and present day logical strategies including the use of refined instruments like GC, HPLC, NMR, GC-MS, and LC-MS and so on for medications, pharmaceuticals and others for an investigational new drug to initiate clinical trials on humans, and may include the step of obtaining regulatory approval with a new drug application to market the drug.

Recommended: WORLD PHARMA CONGRESS 2018 | PHARMA FORMULATIONS 2018 | PHARMA RESEARCH 2019 | PHARMA NANO 2019

Related Conferences: 11th World Congress on Pharmaceutical Sciences, September 28-29, 2018, Montreal, Canada, 15th International Conference on Pharmaceutical Formulations & Drug Delivery, September 17-18, 2018, Philadelphia, Pennsylvania, USA, 2nd International Conference & B2B on Pharma Research and Development, April 26-27, 2019, Houston, USA, 2nd International Conference and Exhibition on Pharmaceutical Nanotechnology and Nanomedicine, March 20-21, 2019, New York , USA, 9th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR, March 20-21, 2019 Houston, USA, Annual Bio analytical Conference, July 9-12, 2018, Madison, Wisconsin, USA, AAPS Pharma Sci360, November 4-7, 2018, Washington,USA

Related Societies USA: American Association of Pharmaceutical Scientists, Association of Clinical Research Organizations, Pharmaceutical Research and Manufacturers of America

Related Societies Europe: The European Federation For Pharmaceutical Sciences, Pharmaceutical Group of the European Union, Association of the British Pharmaceutical Industry

Related Societies Asia Pacific: Federation of Asian Pharmaceutical Associations, Pharmaceutical Research and Manufacturers Association, International Pharmaceutical Manufacturers Group

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.

Recommended: WORLD PHARMA CONGRESS 2018 | PHARMA FORMULATIONS 2018 | PHARMA RESEARCH 2019 | PHARMA NANO 2019

Related Conferences: 11th World Congress on Pharmaceutical Sciences, September 28-29, 2018, Montreal, Canada, 15th International Conference on Pharmaceutical Formulations & Drug Delivery, September 17-18, 2018, Philadelphia, Pennsylvania, USA, 2nd International Conference & B2B on Pharma Research and Development, April 26-27, 2019, Houston, USA, 2nd International Conference and Exhibition on Pharmaceutical Nanotechnology and Nanomedicine, March 20-21, 2019, New York , USA, 9th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR, March 20-21, 2019 Houston, USA, Annual Bio analytical Conference, July 9-12, 2018, Madison, Wisconsin, USA, AAPS Pharma Sci360, November 4-7, 2018, Washington,USA

Related Societies USA: American Association of Pharmaceutical Scientists, Association of Clinical Research Organizations, Pharmaceutical Research and Manufacturers of America

Related Societies Europe: The European Federation For Pharmaceutical Sciences, Pharmaceutical Group of the European Union, Association of the British Pharmaceutical Industry

Related Societies Asia Pacific: Federation of Asian Pharmaceutical Associations, Pharmaceutical Research and Manufacturers Association, International Pharmaceutical Manufacturers Group

Track 4: Quality Control and Regulation

Quality control, or QC for short, is a procedure by which elements audit the quality of all elements engaged with creation. ISO 9000 characterizes quality control as "A piece of quality administration concentrated on satisfying quality necessities". New Drugs are developed at an accelerated rate and the drug marketed should be safe, so many sophisticated and analytical methods are being developed for their evaluation to help the patients with a safe medication.

Recommended: WORLD PHARMA CONGRESS 2018 | PHARMA FORMULATIONS 2018 | PHARMA RESEARCH 2019 | PHARMA NANO 2019

Related Conferences: 11th World Congress on Pharmaceutical Sciences, September 28-29, 2018, Montreal, Canada, 15th International Conference on Pharmaceutical Formulations & Drug Delivery, September 17-18, 2018, Philadelphia, Pennsylvania, USA, 2nd International Conference & B2B on Pharma Research and Development, April 26-27, 2019, Houston, USA, 2nd International Conference and Exhibition on Pharmaceutical Nanotechnology and Nanomedicine, March 20-21, 2019, New York , USA, 9th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR, March 20-21, 2019 Houston, USA, Annual Bio analytical Conference, July 9-12, 2018, Madison, Wisconsin, USA, AAPS Pharma Sci360, November 4-7, 2018, Washington,USA

Related Societies USA: American Association of Pharmaceutical Scientists, Association of Clinical Research Organizations, Pharmaceutical Research and Manufacturers of America

Related Societies Europe: The European Federation For Pharmaceutical Sciences, Pharmaceutical Group of the European Union, Association of the British Pharmaceutical Industry

Related Societies Asia Pacific: Federation of Asian Pharmaceutical Associations, Pharmaceutical Research and Manufacturers Association, International Pharmaceutical Manufacturers Group

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.

Recommended: WORLD PHARMA CONGRESS 2018 | PHARMA FORMULATIONS 2018 | PHARMA RESEARCH 2019 | PHARMA NANO 2019

Related Conferences: 11th World Congress on Pharmaceutical Sciences, September 28-29, 2018, Montreal, Canada, 15th International Conference on Pharmaceutical Formulations & Drug Delivery, September 17-18, 2018, Philadelphia, Pennsylvania, USA, 2nd International Conference & B2B on Pharma Research and Development, April 26-27, 2019, Houston, USA, 2nd International Conference and Exhibition on Pharmaceutical Nanotechnology and Nanomedicine, March 20-21, 2019, New York , USA, 9th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR, March 20-21, 2019 Houston, USA, Annual Bio analytical Conference, July 9-12, 2018, Madison, Wisconsin, USA, AAPS Pharma Sci360, November 4-7, 2018, Washington,USA

Related Societies USA: American Association of Pharmaceutical Scientists, Association of Clinical Research Organizations, Pharmaceutical Research and Manufacturers of America

Related Societies Europe: The European Federation For Pharmaceutical Sciences, Pharmaceutical Group of the European Union, Association of the British Pharmaceutical Industry

Related Societies Asia Pacific: Federation of Asian Pharmaceutical Associations, Pharmaceutical Research and Manufacturers Association, International Pharmaceutical Manufacturers Group

Track 6: Medicinal Chemistry in Drug Discovery

Discovery of drug molecules is done by a method called QSAR in Medicinal Chemistry. Currently medicinal chemistry uses the technique of computer aided drug discovery (CAD) to minimize the time taken for drug discovery. It avoids the need to synthesize all the test molecules and also test them on many animals. By use of CAD, the drug molecule and its ability to work on a receptor is predicited.

Recommended: WORLD PHARMA CONGRESS 2018 | PHARMA FORMULATIONS 2018 | PHARMA RESEARCH 2019 | PHARMA NANO 2019

Related Conferences: 11th World Congress on Pharmaceutical Sciences, September 28-29, 2018, Montreal, Canada, 15th International Conference on Pharmaceutical Formulations & Drug Delivery, September 17-18, 2018, Philadelphia, Pennsylvania, USA, 2nd International Conference & B2B on Pharma Research and Development, April 26-27, 2019, Houston, USA, 2nd International Conference and Exhibition on Pharmaceutical Nanotechnology and Nanomedicine, March 20-21, 2019, New York , USA, 9th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR, March 20-21, 2019 Houston, USA, Annual Bio analytical Conference, July 9-12, 2018, Madison, Wisconsin, USA, AAPS Pharma Sci360, November 4-7, 2018, Washington,USA

Related Societies USA: American Association of Pharmaceutical Scientists, Association of Clinical Research Organizations, Pharmaceutical Research and Manufacturers of America

Related Societies Europe: The European Federation For Pharmaceutical Sciences, Pharmaceutical Group of the European Union, Association of the British Pharmaceutical Industry

Related Societies Asia Pacific: Federation of Asian Pharmaceutical Associations, Pharmaceutical Research and Manufacturers Association, International Pharmaceutical Manufacturers Group

Track 7: 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.

Recommended: WORLD PHARMA CONGRESS 2018 | PHARMA FORMULATIONS 2018 | PHARMA RESEARCH 2019 | PHARMA NANO 2019

Related Conferences: 11th World Congress on Pharmaceutical Sciences, September 28-29, 2018, Montreal, Canada, 15th International Conference on Pharmaceutical Formulations & Drug Delivery, September 17-18, 2018, Philadelphia, Pennsylvania, USA, 2nd International Conference & B2B on Pharma Research and Development, April 26-27, 2019, Houston, USA, 2nd International Conference and Exhibition on Pharmaceutical Nanotechnology and Nanomedicine, March 20-21, 2019, New York , USA, 9th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR, March 20-21, 2019 Houston, USA, Annual Bio analytical Conference, July 9-12, 2018, Madison, Wisconsin, USA, AAPS Pharma Sci360, November 4-7, 2018, Washington,USA

Related Societies USA: American Association of Pharmaceutical Scientists, Association of Clinical Research Organizations, Pharmaceutical Research and Manufacturers of America

Related Societies Europe: The European Federation For Pharmaceutical Sciences, Pharmaceutical Group of the European Union, Association of the British Pharmaceutical Industry

Related Societies Asia Pacific: Federation of Asian Pharmaceutical Associations, Pharmaceutical Research and Manufacturers Association, International Pharmaceutical Manufacturers Group

Track 8: Clinical Trials and Regulatory Affairs

Clinical trial generates data on safety and efficacy. Such consequent biomedical or behavioral research studies on human participants are designed to answer specific questions about biomedical or behavioral interferences, including new treatments such as novel vaccines, drugs, dietary supplements, and medical devices. These trials produce data on safety and efficacy. The regulatory affairs outsourcing market has been segmented into five major service sections .Those sections include regulatory affairs, clinical trial applications and product registrations, regulatory writing and publishing, regulatory consulting and legal representation and others. The market sections have been broadly scheduled on the source of their usefulness, efficacy, and generated revenue and geographic revenue.

Recommended: WORLD PHARMA CONGRESS 2018 | PHARMA FORMULATIONS 2018 | PHARMA RESEARCH 2019 | PHARMA NANO 2019

Related Conferences: 11th World Congress on Pharmaceutical Sciences, September 28-29, 2018, Montreal, Canada, 15th International Conference on Pharmaceutical Formulations & Drug Delivery, September 17-18, 2018, Philadelphia, Pennsylvania, USA, 2nd International Conference & B2B on Pharma Research and Development, April 26-27, 2019, Houston, USA, 2nd International Conference and Exhibition on Pharmaceutical Nanotechnology and Nanomedicine, March 20-21, 2019, New York , USA, 9th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR, March 20-21, 2019 Houston, USA, Annual Bio analytical Conference, July 9-12, 2018, Madison, Wisconsin, USA, AAPS Pharma Sci360, November 4-7, 2018, Washington,USA

Related Societies USA: American Association of Pharmaceutical Scientists, Association of Clinical Research Organizations, Pharmaceutical Research and Manufacturers of America

Related Societies Europe: The European Federation For Pharmaceutical Sciences, Pharmaceutical Group of the European Union, Association of the British Pharmaceutical Industry

Related Societies Asia Pacific: Federation of Asian Pharmaceutical Associations, Pharmaceutical Research and Manufacturers Association, International Pharmaceutical Manufacturers Group

Track 9: 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.

Recommended: WORLD PHARMA CONGRESS 2018 | PHARMA FORMULATIONS 2018 | PHARMA RESEARCH 2019 | PHARMA NANO 2019

Related Conferences: 11th World Congress on Pharmaceutical Sciences, September 28-29, 2018, Montreal, Canada, 15th International Conference on Pharmaceutical Formulations & Drug Delivery, September 17-18, 2018, Philadelphia, Pennsylvania, USA, 2nd International Conference & B2B on Pharma Research and Development, April 26-27, 2019, Houston, USA, 2nd International Conference and Exhibition on Pharmaceutical Nanotechnology and Nanomedicine, March 20-21, 2019, New York , USA, 9th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR, March 20-21, 2019 Houston, USA, Annual Bio analytical Conference, July 9-12, 2018, Madison, Wisconsin, USA, AAPS Pharma Sci360, November 4-7, 2018, Washington,USA

Related Societies USA: American Association of Pharmaceutical Scientists, Association of Clinical Research Organizations, Pharmaceutical Research and Manufacturers of America

Related Societies Europe: The European Federation For Pharmaceutical Sciences, Pharmaceutical Group of the European Union, Association of the British Pharmaceutical Industry

Related Societies Asia Pacific: Federation of Asian Pharmaceutical Associations, Pharmaceutical Research and Manufacturers Association, International Pharmaceutical Manufacturers Group

Track 10: Proteomic analysis

Proteomic analysis refers to the systematic identification and quantification of the complete complement of proteins of a biological system at a specific point in time. Mass spectrometry is the technique most often used for proteomic analysis. This study is a basis for the discovery of new drugs which aim to find new drugs to inactivate proteins involved in the disease. Researchers expect to use these techniques to develop personalized drugs that are more effective for the individual.

Recommended: WORLD PHARMA CONGRESS 2018 | PHARMA FORMULATIONS 2018 | PHARMA RESEARCH 2019 | PHARMA NANO 2019

Related Conferences: 11th World Congress on Pharmaceutical Sciences, September 28-29, 2018, Montreal, Canada, 15th International Conference on Pharmaceutical Formulations & Drug Delivery, September 17-18, 2018, Philadelphia, Pennsylvania, USA, 2nd International Conference & B2B on Pharma Research and Development, April 26-27, 2019, Houston, USA, 2nd International Conference and Exhibition on Pharmaceutical Nanotechnology and Nanomedicine, March 20-21, 2019, New York , USA, 9th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR, March 20-21, 2019 Houston, USA, Annual Bio analytical Conference, July 9-12, 2018, Madison, Wisconsin, USA, AAPS Pharma Sci360, November 4-7, 2018, Washington,USA

Related Societies USA: American Association of Pharmaceutical Scientists, Association of Clinical Research Organizations, Pharmaceutical Research and Manufacturers of America

Related Societies Europe: The European Federation For Pharmaceutical Sciences, Pharmaceutical Group of the European Union, Association of the British Pharmaceutical Industry

Related Societies Asia Pacific: Federation of Asian Pharmaceutical Associations, Pharmaceutical Research and Manufacturers Association, International Pharmaceutical Manufacturers Group

Track 11: 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.

Recommended: WORLD PHARMA CONGRESS 2018 | PHARMA FORMULATIONS 2018 | PHARMA RESEARCH 2019 | PHARMA NANO 2019

Related Conferences: 11th World Congress on Pharmaceutical Sciences, September 28-29, 2018, Montreal, Canada, 15th International Conference on Pharmaceutical Formulations & Drug Delivery, September 17-18, 2018, Philadelphia, Pennsylvania, USA, 2nd International Conference & B2B on Pharma Research and Development, April 26-27, 2019, Houston, USA, 2nd International Conference and Exhibition on Pharmaceutical Nanotechnology and Nanomedicine, March 20-21, 2019, New York , USA, 9th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR, March 20-21, 2019 Houston, USA, Annual Bio analytical Conference, July 9-12, 2018, Madison, Wisconsin, USA, AAPS Pharma Sci360, November 4-7, 2018, Washington,USA

Related Societies USA: American Association of Pharmaceutical Scientists, Association of Clinical Research Organizations, Pharmaceutical Research and Manufacturers of America

Related Societies Europe: The European Federation For Pharmaceutical Sciences, Pharmaceutical Group of the European Union, Association of the British Pharmaceutical Industry

Related Societies Asia Pacific: Federation of Asian Pharmaceutical Associations, Pharmaceutical Research and Manufacturers Association, International Pharmaceutical Manufacturers Group

Track 12: Pharmaceutical Nanotechnology

Pharmaceutical Nanotechnology embraces applications of nanoscience to pharmacy as nanomaterials, and as devices like drug delivery, diagnostic, imaging and biosensor. Pharmaceutical nanotechnology plays an important role in drug discovery and development as it helps in the improving the characteristics such as solubility, bioavailability, etc…of the potent drugs and excipients etc. The global nanotechnology drug delivery market was valued at US$ 41,062.5 Mn in 2014 and is projected to reach US$ 118,527.2 Mn by 2023, expanding at a CAGR of 12.5% from 2015 to 2023. Rising incidence of chronic diseases such as cancer and diabetes in the region fueled the growth of the nanotechnology drug delivery market.

Recommended: WORLD PHARMA CONGRESS 2018 | PHARMA FORMULATIONS 2018 | PHARMA RESEARCH 2019 | PHARMA NANO 2019

Related Conferences: 11th World Congress on Pharmaceutical Sciences, September 28-29, 2018, Montreal, Canada, 15th International Conference on Pharmaceutical Formulations & Drug Delivery, September 17-18, 2018, Philadelphia, Pennsylvania, USA, 2nd International Conference & B2B on Pharma Research and Development, April 26-27, 2019, Houston, USA, 2nd International Conference and Exhibition on Pharmaceutical Nanotechnology and Nanomedicine, March 20-21, 2019, New York , USA, 9th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR, March 20-21, 2019 Houston, USA, Annual Bio analytical Conference, July 9-12, 2018, Madison, Wisconsin, USA, AAPS Pharma Sci360, November 4-7, 2018, Washington,USA

Related Societies USA: American Association of Pharmaceutical Scientists, Association of Clinical Research Organizations, Pharmaceutical Research and Manufacturers of America

Related Societies Europe: The European Federation For Pharmaceutical Sciences, Pharmaceutical Group of the European Union, Association of the British Pharmaceutical Industry

Related Societies Asia Pacific: Federation of Asian Pharmaceutical Associations, Pharmaceutical Research and Manufacturers Association, International Pharmaceutical Manufacturers Group

Track 13: Computer aided Drug Design

Drug Design through computer, a most recent, exceptionally viable strategy in present day field. Presently a day’s Computer Aided Drug Design (CADD) apparatuses are pushed off in nanotechnology, atomic science, organic chemistry and so on. The principle advantage of the CADD is added up to viable in innovative work of drugs. There are wide scopes of programming are utilized as a part of CADD, Network processing, window made general PBPK/PD demonstrating programming, PKUDDS for structure based drug design, APIS, JAVA, Perl and Python, CADD and programming including programming libraries. There are distinctive systems utilized as a part of CADD perception, homology, atomic energetic, vitality minimization sub-atomic docking, QSAR and so on. Drug design gathering 2016 gives a phase to fundamentally dissect and understand the strategies and components and Computer aided drug design is appropriate in Tumor illness, transport of drug to particular site in body, information accumulations and stockpiles of organics and natural.

The market size and estimate in USD million for every service type for the period from 2010 -2020, considering 2013 as basic year. This report also delivers the compounded annual growth rate (CAGR %) for each market segment for the forecast period from 2014- 2020.

Recommended: WORLD PHARMA CONGRESS 2018 | PHARMA FORMULATIONS 2018 | PHARMA RESEARCH 2019 | PHARMA NANO 2019

Related Conferences: 11th World Congress on Pharmaceutical Sciences, September 28-29, 2018, Montreal, Canada, 15th International Conference on Pharmaceutical Formulations & Drug Delivery, September 17-18, 2018, Philadelphia, Pennsylvania, USA, 2nd International Conference & B2B on Pharma Research and Development, April 26-27, 2019, Houston, USA, 2nd International Conference and Exhibition on Pharmaceutical Nanotechnology and Nanomedicine, March 20-21, 2019, New York , USA, 9th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR, March 20-21, 2019 Houston, USA, Annual Bio analytical Conference, July 9-12, 2018, Madison, Wisconsin, USA, AAPS Pharma Sci360, November 4-7, 2018, Washington,USA

Related Societies USA: American Association of Pharmaceutical Scientists, Association of Clinical Research Organizations, Pharmaceutical Research and Manufacturers of America

Related Societies Europe: The European Federation For Pharmaceutical Sciences, Pharmaceutical Group of the European Union, Association of the British Pharmaceutical Industry

Related Societies Asia Pacific: Federation of Asian Pharmaceutical Associations, Pharmaceutical Research and Manufacturers Association, International Pharmaceutical Manufacturers Group

Track 14: 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.

Recommended: WORLD PHARMA CONGRESS 2018 | PHARMA FORMULATIONS 2018 | PHARMA RESEARCH 2019 | PHARMA NANO 2019

Related Conferences: 11th World Congress on Pharmaceutical Sciences, September 28-29, 2018, Montreal, Canada, 15th International Conference on Pharmaceutical Formulations & Drug Delivery, September 17-18, 2018, Philadelphia, Pennsylvania, USA, 2nd International Conference & B2B on Pharma Research and Development, April 26-27, 2019, Houston, USA, 2nd International Conference and Exhibition on Pharmaceutical Nanotechnology and Nanomedicine, March 20-21, 2019, New York , USA, 9th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR, March 20-21, 2019 Houston, USA, Annual Bio analytical Conference, July 9-12, 2018, Madison, Wisconsin, USA, AAPS Pharma Sci360, November 4-7, 2018, Washington,USA

Related Societies USA: American Association of Pharmaceutical Scientists, Association of Clinical Research Organizations, Pharmaceutical Research and Manufacturers of America

Related Societies Europe: The European Federation For Pharmaceutical Sciences, Pharmaceutical Group of the European Union, Association of the British Pharmaceutical Industry

Related Societies Asia Pacific: Federation of Asian Pharmaceutical Associations, Pharmaceutical Research and Manufacturers Association, International Pharmaceutical Manufacturers Group

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.

Past Conferences

We are delighted to all our Organizing Committee Members, Keynote Speakers, Speakers, Delegates, Students, Exhibitor and Media partners for making our Past Pharmaceutical Analysis 2018Conference in USA Region with great Pride.

International Conference on Pharmaceutical Analysis and Quality Control Strategies, June 27-28, 2018

Venue: Pacific Gateway Hotel at Vancouver Airport, 3500 Cessna Drive Richmond, British Columbia V7B 1C7 Canada

Past Conference Report

Pharmaceutical Analysis 2018 Report:

Conference Series LLC Ltd successfully hosted the International Conference on Pharmaceutical Analysis and Quality Control Strategies during June 27-28, 2018 at Vancouver, Canada. The conference focused on the theme “Analytical Techniques for Analysis of Pharmaceutical Products”. The conference was successful in gathering eminent speakers from various reputed organizations and their paramount talks enlightened the gathering.

The pragmatic meet organized by Conference Series LLC Ltd received generous response from the Editorial Board Members of Journals as well as expertise from academia, talented researchers and young student community. Researchers and students who attended from different parts of the world made the conference one of the most successful events in 2018 from Conference Series Group. The conference was marked with the presence of renowned Speakers, Young Researchers, Students and Business Delegates driving the two day event into the path of success with thought provoking keynote and plenary presentations.

Pharmaceutical Analysis 2018 is designed to offer comprehensive range of sessions that includes Drug Discovery and Development, Analytical Methods and Control Strategies, Pharmaceutical Nanotechnology and many more

  1. Analytical Methods and Control Strategies
  2. Drug Discovery & Development
  3. Analytical Method Development and Validation
  4. Modern Pharmaceutical Analysis
  5. Chromatography & Separation Techniques
  6. Quality Control of Analytical Methods
  7. Errors in pharmaceutical analysis & statistical validation
  8. Electroanalytical Methods
  9. Analysis of Pharmaceutical Agents
  10. GLP and GMP Method Development, Validation and Remediation
  11. Pharmaceutical and Biomedical Analysis
  12. Pharmaceutical Microbiology
  13. Preformulation Studies
  14. Biopharmaceutical Research & Development Process
  15. Pharmaceutical Nanotechnology

The proceedings of the conference were embarked with an Opening Ceremony followed by a series of Lectures delivered by both Honourable Guests and members of the Keynote forum. The adepts who promulgated the theme with their exquisite talks were:

  1. Steinar Madsen -  Norwegian Medicines Agency, Norway
  2. Steven J. Durham -   Labaton Sucharow LLP, USA
  3. Kooros Motamed-Larijani - NantBioscience Inc , USA
  4. Yara Peluso Cid- Federal Rural University of Rio de Janeiro, Brazil
  5. Eric Ka Wai Hui - ArmaGen, USA
  6. Marika Kamberi -Abbott Vascular, USA
  7. Gregory K Bell - Charles River Associates, USA
  8. Yite Robert Chou - Merck & Co Inc., USA
  9. Mandla S Makhanya - University of South Africa, South Africa

We extend our heartiest thanks to all the Organizing Committee Members for their kind support rendered towards the success of Pharmaceutical Analysis 2018. At the same time we take the opportunity to thank all the speakers, delegates and participants for providing their valuable contribution and time for Pharmaceutical Analysis 2018.

Pharmaceutical Analysis 2018 Organizing Committee would like to thank the Chairs and Co-Chairs of the conference, Yite Robert Chou, Kooros Motamed-Larijani, Mandla S Makhanya, who contributed a lot for the smooth functioning of this event.

Keynote Speakers

Past Conference Keynote Speakers

Our warm gratitude to all the Honorable Keynote Speakers of Pharmaceutical Analysis 2018:

 Steinar Madsen - Medical Director, Norwegian Medicines Agency, Norway

Steven J. Durham - Partner  Labaton Sucharow, USA

Kooros Motamed Larijani - Director Drug Development, NantBioscience Inc , USA

Yara Peluso Cid - Federal Rural University of Rio de Janeiro, Brazil

Eric Ka Wai Hui - Vice President & Cofounder-ArmaGen, USA

Marika Kamberi  - Abbott Vascular, USA

Gregory K Bell - Charles River Associates, USA

Yite Robert Chou - Merck & Co Inc., USA

Mandla S Makhanya - University of South Africa, South Africa

Media Partners

Media Partners

Conference series LLC Ltd offers Special thanks to the organizations like Tabeeby, Conference Clocate, who supported the conferences by promoting in various modes online and offline which helped the conferences reach every nook and corner of the globe.

*** Bookmark Your Dates for the forthcoming Conference; we are hoping to see you soon! ***

Market Analysis

The global Pharmaceutical Analytical testing market size was valued at USD 4.4 billion in 2015 and it is estimated to grow with CAGR of 8.1% over the forecast period. Increasing R&D investments, increasing focus on the product quality & safety, regulation are vital drivers of growth of the market. Increasing R&D investments is one of the critical sustainability strategies. In the recent years, the R&D expense is increasing and expected to continue to increase over the forecast period. The pharmaceuticals industry is dominated by the U.S., which holds around 45% of the global market share because it is driven by the regulatory scenario and the presence of well-established outsourcing infrastructure. Leading industry players designate around 20% of their turnover to R&D to maintain a competitive edge. Increase in complexity and number of standards, which a single product may have to comply with, is driving substantial growth in the pharmaceutical analytical testing services outsourcing market. Moreover, international organizations such as the International Council for Harmonization (ICH) give harmonized guidelines that are regularly updated, so companies are required to stay align with regulatory updates and avail expertise & advisory services to be in synchronization with evolving standards.

U.S. pharmaceutical analytical testing market, 2014 - 2025 (USD Billion)

 

Past Conference Chairs/ Co-Chairs

Past Conference Chairs/Co-Chairs:

It is our Pleasure to show our appreciation towards our Chairs/Co-Chairs for the Sessions, namely

Yite Robert Chou, Merck & Co Inc., USA

Kooros Motamed Larijani - Director Drug Development, NantBioscience Inc , USA

Mandla S Makhanya, University of South Africa, South Africa

 

To Collaborate Scientific Professionals around the World

Conference Date June 28-29, 2019 San Diego, USA

For Sponsors & Exhibitors

[email protected]

Speaker Opportunity

Supported By

Journal of Bioequivalence & Bioavailability

Pharmaceutica Analytica Acta

International Journal of Drug Development and Research

All accepted abstracts will be published in respective Conference Series LLC LTD International Journals.

Abstracts will be provided with Digital Object Identifier by