Golden, Colorado: July 15, 2014

I will be presenting an “Overview of Recent FDA Enforcement Activities in Dietary Supplements” at this FREE PerkinElmer event focused on “Analytical Testing of Pharmaceuticals, Dietary Supplements, and Botanicals“. The meeting is focused on quality control for pharmaceutical and dietary supplement manufacturers and includes sessions on heavy metals testing, and correct use of FTIR for botanical ingredients. The seminar will be held on July 15 in Golden (at the Denver Marriott West, Colorado) .

Agenda and FREE Registration: http://www.eventbrite.com/e/nutrapharma-seminar-golden-co-tickets-11922188587

Abstract for my session (scheduled after lunch):

“Good Manufacturing Practices for Dietary Supplements (21 CFR Part 111) have now been in place for over 5 years.  FDA recently stated that around 70% of dietary supplement firms inspected so far have been found to have one or more CGMP defects or violations.  FDA periodically releases information on its enforcement activities, such as inspection observations provided to firms via 483’s, and Warning Letters.  This presentation gives an overview on what these data reveal about industry compliance, with a focus on laboratory operations, testing, and analytical methods”.

See flyer for more details of the other sessions.

Hope to see you there!