Dissolution Testing: Methods, Validation and Regulations

January 28, 2015

CfPA-The Center for Professional Advancement, Amsterdam, The Netherlands
11-12 June 2015

Who Should Attend?
This course contains a comprehensive coverage of the science and practice of dissolution testing in pharmaceutical, biotechnology, cosmetic and related industries, and is designed to benefit professionals in the following areas:

  • Pharmaceutical/biotechnology product development
  • Quality control and quality assurance
  • Regulatory affairs
  • Analytical support
  • Product stability testing

Course Description

This 2-day, intensive course focuses on the science and principles concerning dissolution of pharmaceutical, biotechnology and cosmetic products. The contents of the course contain an in-depth discussion on the background and theory of dissolution, purpose and classification of dissolution methods and regulatory requirements for dissolution testing. Current FDA and ICH guidelines on dissolution will be discussed. A comprehensive detail is provided on dissolution method development, dissolution media and selection of the method. Product specific dissolution testing is included in the discussion. The course includes several case studies and a detailed workshop on dissolution method development and data analyses.

Maximize Your Learning!
Attend this course and its Companion Course:
Drug Product Stability and Shelf-Life
8-10 June 2015 • 8-10 June • Course ID #599

Organized by:

CfPA-The Center for Professional Advancement

Invited Speakers:

Dr. Pardeep K. Gupta; Professor of Pharmaceutics, Philadelphia College of Pharmacy, University of The Sciences in Philadelphia (USP)

Dr. Pardeep K. Gupta is a Professor of Pharmaceutics in Philadelphia College of Pharmacy at the University of The Sciences in Philadelphia (USP). He received his B. Pharm. and M. Pharm. (pharmaceutical chemistry) degrees from India. He also received a M.S. degree in medicinal chemistry from USP and his Ph.D. in pharmaceutics from University of Wisconsin. His research interests include delivery of proteins and peptides and study of the interaction of drugs with biomembranes. He has published several articles and has authored several book chapters. His teaching responsibilities include courses in solubility, controlled drug delivery and drug stability at the graduate level. He has served on the editorial board of Remington: The Science and Practice of Pharmacy, as the editor of Pharmaceutical Chemistry and Pharmaceutical Testing, Analysis and Control sections of the book, and as author of two chapters.

Deadline for Abstracts:

n/a

Registration:

Please click here for registration information.

E-mail:

sberg@cfpa.com

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