Challenges in Dissolution Workshop

Overview

A discussion of issues associated with dissolution testing of pharmaceutical dosage forms—such as semisolid dosage forms applied to the skin, liquid-filled capsules, and gelatin capsules—and of other products, such as botanicals and dietary supplements.

Objectives of the Workshop

  1. To present the USP activities regarding the development of new General Chapters (<1724> and <1094>), revisions to some current USP General Chapters (<711> and <2040>), and Performance Verification Testing (PVT)
  2. To collect comments and suggestions on the major USP projects related to dissolution testing
  3. To identify possible collaborators to participate in these USP projects

Preliminary Agenda

When: June 11–12, 2012
Where: USP Headquarters, Meetings Center, Rockville, MD

Registration Fees & Information

Register Online Now!

  • Early Bird: If registered on or before May 11: Industry—$495; Association/Academia/Government—$295
  • Regular: Industry—$595;  Association/Academia/Government—$395
  • Group Discounts: Available for three or more attendees from the same company. Contact conferences@usp.org for details.

Registration fee includes full two-day program, meeting materials, continental breakfast and lunch each day, and a networking reception.

Who Should Participate:

  • Scientists Responsible for Developing Dissolution Tests
  • Regulatory Affairs Scientists
  • Formulators
  • Metrology Scientists
  • Validation Scientists
  • Dietary Supplement Manufacturers

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