The FDA and Cosmetic Oversight - What does that look like?

"The FDA and Cosmetic Oversight - What does that look like?" is a training session aimed at providing participants with an understanding of the role of the Food and Drug Administration (FDA) in regulating cosmetics. The training covers various aspects, including the definition and purpose of cosmetics, the FDA's authority and responsibilities, regulatory requirements, safety considerations, and emerging issues in the cosmetic industry.

The training begins with an introduction to cosmetics, highlighting their purpose and the different types available. It emphasizes the benefits and potential risks associated with cosmetic usage and addresses common misconceptions and industry challenges.

Participants then learn about the FDA's role in cosmetic oversight. This includes an overview of the FDA's authority, the impact of the Federal Food, Drug, and Cosmetic Act, - focusing on the new Modernization of Cosmetics Regulation Act of 2022 (MoCRA) and the limitations of the FDA's regulatory power.

The training will explore Good Manufacturing Practices (GMPs) for cosmetic manufacturers. The safety of cosmetics and adverse event reporting are discussed, including the Cosmetic Ingredient Review process and the FDA's actions in response to reported safety concerns. The training also addresses challenges and concerns in cosmetic oversight, such as product safety, contamination, mislabeling, and deceptive marketing practices.