Dietary Supplements 21 CFR 111 Regulations
Learn about the FDA regulations for facility and product compliance with 21 CFR 111 Dietary Supplements rule. This training will cover Subparts A-P to further understand the requirements, how to develop effective programs, the importance of the Quality role, and avoiding compliance issues. We will explore what are MMRs, BPRs, and recording keeping requirements. We will also briefly cover dietary supplement labeling, claims, and the future of regulations.
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Learning Objectives:
- Be able to understand what are Dietary Supplements and distinction in the marketplace
- Understand all subparts of21 CFR 111 and how it impacts your facility and products
- Learn how to develop, implement, and maintain effective programs required for compliance
- Discuss the importance of Quality in a dietary supplement operation
- Learn the basics of labeling and claims regulations to avoid compliance or litigation issues
- Be able to prepare your team to comply with FDA and third-party audit requirements
Who Should Attend:
Quality Assurance/Control Teams, Food Safety, Regulatory & Labeling Specialists, and anybody that has a managerial role in developing, implementing, and maintaining a facility and its products that are subject to Dietary Supplement regulations.
Prerequisites:
None.
