This is a CRN Associate Member Spotlight. Learn more: EASConsultingGroup.com
EAS Consulting Group invites CRN members to participate in its upcoming virtual training series, Dietary Supplement Good Manufacturing Practices (GMP) Compliance Seminar:
- Oct. 14, 16, 21, and 23 from 11:00 am–4:00 pm Eastern
Shelly Blackwell, EAS senior director for dietary supplement and tobacco services who will lead the seminar with Jeb Hunter, EAS senior regulatory consultant, recently spoke with NutraIngredients-USA, describing a significant shift in FDA enforcement priorities.
FDA now increasingly inspects not just manufacturers, but brand owners and even their corporate offices—a crucial reminder that GMP requirements apply to all brand owners, not just those with direct manufacturing operations, she notes.
For more than a decade, supplement GMPs outlined in 21 CFR 111 have shaped the dietary supplement industry. Yet FDA continues to issue Warning Letters citing firms for failure to comply with even the most fundamental requirements. With heightened regulatory oversight, EAS Consulting’s upcoming seminar provides timely, practical guidance for companies seeking to strengthen compliance, prepare for inspections, and ensure product quality.
The EAS seminar is ideal for:
- Executives and staff involved in management, regulatory affairs, quality control/assurance, labeling, packaging, storage, and distribution of dietary supplements.
- Consultants, auditors, attorneys, and others seeking a comprehensive understanding of dietary supplement GMPs and how they apply in practice.
Seminar participants will gain:
- A detailed review of 21 CFR 111 requirements and other applicable statutes.
- Practical guidance on applying GMPs to your facility.
- Coaching on how to prepare for FDA inspections and avoid Form FDA 483 observations.
- Hands-on group work sessions to reinforce GMP understanding.
Learn more and register via the EAS Consulting website.