Ever wonder what the most important critical quality attributes are for pharmaceutical excipients? How does USP organize mandatory identification tests and assays, along with non-mandatory tests for excipient characteristics? What’s the difference between a monograph and a general chapter? Answers to these questions and more can be found in the videos on this page, from a live presentation at the AAPS 2017 Annual Meeting by USP Senior Scientific Liaison, Dr. Galina Holloway.
For more information on USP’s work with Pharmaceutical Excipients, please visit USP’s Excipients page. To receive periodic updates from USP Excipients, please visit our newsletter signup page and choose “Excipients Updates”.