Date: August 14, 2026
Time: 1:00 p.m. Eastern
FDA’s Experts Dive Into Nitty-Gritty of Establishing and Verifying Product Specifications under 21 CFR Part 111
Siobhan Gallagher Taylor and Gary Pecic, FDA’s national experts on dietary supplements, will lead this one-hour cGMP webinar.
Ms. Taylor and Mr. Pecic will offer an overview of the relevant rules governing finished product specifications, report FDA data trends, and provide hands-on, real-world examples to help manufacturers and brands meet the relevant requirements in 21 CFR Part 111.
Join this webinar to:
– Understand from FDA’s perspective the importance of establishing and meeting finished product specifications, and how these requirements fit into the five pillars of a compliant dietary supplement quality system.
– Learn about FDA product specification data trends and the associated risks of getting 483s, warning letters and injunctions for noncompliance.
– Gain practical guidance from FDA’s leading experts on establishing and meeting finished product specifications.
– Get answers to your questions from FDA.
Webinar Agenda
1:00 p.m. – 1:45 p.m. Eastern
Siobhan Gallagher Taylor and Gary Pecic, FDA’s national experts on dietary supplements in the Office of Human Food Inspectorate, present on establishing and meeting finished product specifications.
1:45 p.m. – 2:00 p.m. Eastern
Q&A with Ms. Taylor and Mr. Pecic, moderated by NPA VP of regulatory affairs and communications, Josh Long.
Price:
NPA Members: FREE
Non-Members: $100
