FDA Grand Rounds - Postmarket Regulation of Cosmetic Products: The Who, What, When, Why, and How

Join FDA experts from the Office of Cosmetics and Colors for a comprehensive presentation on cosmetic product regulation in the United States. This session provides essential information about the Modernization of Cosmetics Regulation Act (MoCRA), landmark legislation passed in December 2022 that gave FDA significant new authority over cosmetics for the first time since 1938. What You'll Learn: • U.S. cosmetics regulatory framework and FDA's statutory authority • Facility registration and product listing requirements under MoCRA • Adverse event reporting procedures for industry and consumers • Good Manufacturing Practices (GMP) regulations and safety substantiation • New labeling requirements, including professional-use designations and contact information • Mandatory recall authority and records inspection provisions • Small business exemptions and compliance deadlines