Pharmaceutical Analysis

Regulatory Affairs has a very specific meaning within the healthcare industries. Its regulations are for systematic manufacturing and marketing of safe, efficacious and qualitative drugs. Improving new regulations and adapting to the technology regulatory affairs set new goals and challenges to the pharmaceutical formulation. The global regulatory affairs outsourcing market had a valuation of US$1.9 bn in 2014. The market is expected to expand at a substantial 11.5% CAGR from 2015 to 2023 and rise to a valuation of US$5.7 billion by 2023.

  • Novel approaches to analytical and bioanalytical methods
  • Bioanalytical techniques
  • Chromatography and techniques
  • Spectroscopic techniques
  • Nuclear magnetic resonanace
  • Mass spectroscopy
  • Regulatory issues and biosafety challenges in bioanalysis
  • Applications of analytical and bioanalytical methods

Related Conference of Pharmaceutical Analysis

June 06-07, 2018

International Conference & B2B on Pharma Research and Development

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August 20-21, 2018

12th Asian Biologics and Biosimilars Congress

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October 18-20, 2018

18th World Pharma Congress

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14th International Conference on Generic Drugs and Biosimilars

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6 th European Biopharma Congress

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