21 CFR 111 Dietary Supplement GMP Overview

FDA expects all companies that manufacture, package or hold dietary supplement products to follow 21 CFR 111, the Dietary Supplement current Good Manufacturing Practices (cGMPs). Combining extensive industry experience and concrete understanding of regulations with flexible and convenient training, this course provides a solid understanding of cGMPs and the responsibilities expected for various individuals and groups within the company. You will learn how to apply cGMP principles to specific situations.

The 21 CFR 111 GMP training is interactive, with hands-on exercises including case studies from recent warning letters. Bring your questions and prepare to interact with the instructor and your peers in the industry.

This dietary supplement GMP training course provides an overview of subparts A-P of the 21 CFR 111 regulation, including:

• Specifications
• Master manufacturing records/batch production records (MMR/BPR)
• Quality and FDA authority
• Warning letters
• How to make sense of complex regulations in an understandable and comprehensive manner
• How to effectively convert regulations into real-world examples and scenarios, offering clarity and operational success
• How regulations can be applied to your organization in a cost-effective manner