Dietary Supplement GMPs Overview: 21 CFR 111 and Subparts A, P, H and I

This self-paced course provides a brief historical review of regulations in the dietary supplement industry and their evolution as key incidents exposed health and safety risks to the consumer. This eLearning also covers the following subparts of 21 CFR 111, which create the foundation of your quality management system (QMS) and the Good Manufacturing Practices that control product quality:

• Subpart A: General Provisions
• Subpart P: Records and Recordkeeping
• Subpart H: Master Manufacturing Records
• Subpart I: Batch Production Record