Course Overview
This course provides a comprehensive look at the evolving landscape of cosmetic industry regulations, with a focus on safety and claims substantiation under the Modernization of Cosmetics Regulation Act (MOCRA). Through interactive case studies and expert-led discussions, participants will follow the lifecycle of a cosmetic product—from safety assessment and toxicological review to claims evaluation and substantiation. The course highlights key regulatory bodies and frameworks, including the FDA, FTC, Cosmetic Ingredient Review (CIR), and international authorities such as the SCCS, giving attendees a well-rounded understanding of compliance expectations in the current U.S. marketplace.
Building on real-world examples, the program also explores how to navigate issues such as serious adverse event (SAE) reporting, toxicological risk assessment (TRA), and the fine line between cosmetic and drug claims. Participants will gain insight into what constitutes credible evidence, how to design and interpret product testing, and best practices for developing a robust, defensible safety and claims program.
Who Should Attend
This course is designed for professionals working in product development, regulatory affairs, safety assessment, quality assurance, and marketing within the cosmetics and personal care industry. It is particularly valuable for formulators, toxicologists, regulatory specialists, and brand managers who need to understand how evolving U.S. regulations impact product safety standards and claims substantiation. The program is also suitable for newcomers seeking a strong foundation in the legal and regulatory principles that govern cosmetic products in the United States.