Please join us for this FREE dynamic virtual event.
July 15, 9:00am - 12:00pm PST
This non-profit event is hosted by the American Society for Quality, FD&C Division in collaboration with the FDA West. The organizing committee comprised of volunteers from members of the industry: ASQ members, FDA employees, major manufacturers, brand owners, private organizations and consultants.
Hear from the FDA, trade organizations and industry experts on current regulatory updates and industry best practices that impact the dietary supplement industry in the following key areas:
- Update from the FDA Office of Dietary Supplement Programs (ODSP) and NDI
- Botanical Adulteration and Identity Testing
- Development of Food Defense Plan to comply with Intentional Adulteration Rule (IA rules)
- Material Review/Root Cause Analysis/CAPA
Featured Speakers:
Darla Bracy – Keynote Speaker
District Director, San Francisco District
Office of Human & Animal Food s- West Division 5
Food & Drug Administration
Cara Welch, Ph.D – ODSP and NDI update
Director, Office of Dietary Supplements Programs
Center for Food Safety and Applied Nutrition
Food & Drug Administration
Elan Sudberg – Identification Test for Botanicals
CEO, Alkemist Labs
Bhaumik Darji – Botanical Adulteration: Suppliers Program
Quality Manager, Verdure Sciences
Bob Metha – Material Review/Root Cause Analysis/CAPA
ASQ
President, GMP ISO Expert Services
Dan Fabricant, Ph.D - Industry & Regulatory Update
CEO, Natural Products Association
Cathleen Howick - How to Develop a Food Defense Plan
Principal, CEH Consulting
