The FDA regulates both finished dietary supplements and dietary ingredients to ensure they are appropriately labeled, and safe for the consumer. Described in 21 CFR 111, these regulations provide for consistency in the identity, purity, quality, strength and composition of dietary supplements. This lecture-based course provides training on 21 CFR 111, and the current Good Manufacturing Practices (cGMPs) in manufacturing, packaging, labeling and holding operations for dietary supplements. Attention is given to the sixteen subparts, regulatory compliance, and maintaining a culture of quality.
This course is powered and delivered by the CITI Program. To learn more about this course and to register, please visit the CITI Program website.