FDA Grand Rounds - Postmarket Regulation of Cosmetic Products: The Who, What, When, Why, and How
Food and Drug Administration - Office of the Chief Scientist · February 10, 2026
FDA Grand Rounds presenters from the Office of Cosmetics and Colors summarized the Modernization of Cosmetics Regulation Act (MOCRA) provisions, deadlines for good manufacturing practice rules and labeling, facility registration and product listing requirements, and industry obligations for adverse event reporting and recordkeeping.
AI-Generated Content: All content on this page was generated by AI to highlight key points from the meeting. For complete details and context, we recommend watching the full video. so we can fix them.
No transcript available.
No outline available for this source.
No related articles available for this source.
No highlights available for this source.
No claims available for this source.
No actions available for this source.
No topics available for this source.
No clarifying details available for this source.
No discussions available for this source.
No community relevance data available for this source.
No funding sources available for this source.
No speakers available for this source.
No transcript available for this source.
