The Ministry of Food and Drug Safety announced on the 22nd that it will hold an online briefing session on the U.S. 'Cosmetic Modernization Act' by directly inviting officials from the U.S. Food and Drug Administration (FDA) on the 31st.
Companies intending to distribute and sell cosmetics in the U.S. must comply with the U.S. 'Cosmetic Modernization Act,' which has been in effect since December 29 of last year. This includes manufacturing and quality control standards, safety verification, reporting of serious adverse events, facility registration, product listing submission, and labeling requirements.
This briefing session was organized to help domestic companies appropriately respond to the strengthened U.S. cosmetic approval regulations.
The session will provide detailed explanations of the Cosmetic Modernization Act overall, including the mandatory cosmetic facility registration that companies must comply with, and will offer real-time Korean simultaneous interpretation.
Anyone interested in U.S. cosmetic regulations can participate for free after pre-registering through the 'Global Regulatory Harmonization Support Center.'
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