Since 2021, China National Medical Products Administration (NMPA) released and implemented the Cosmetic Supervision and Administration Regulation and a series of subsidiary regulations, reconstructing the entire cosmetics regulatory system. The regulatory focus of NMPA is gradually shifting from the previous emphasis on pre-market approval to the combination of pre-market approval and post-market surveillance.
China's brand-new regulatory system has similarities and differences with the EU's. For European companies or companies already marketing cosmetics in Europe, what differences should be considered before placing cosmetics on the Chinese market? In this webinar, Hedy He from ChemLinked will detail the similarities and differences in basic regulatory information, pre-market requirements, post-market surveillance, company responsibility, etc.
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The presentation deck and recording video will be uploaded to this webpage after the webinar;
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1. Basic Regulatory Information Comparison
2. Pre-market Requirements Comparison
3. Post-market Surveillance Comparison
*The final outline may be subjected to subtle revision.
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ChemLinked Regulatory Analyst
Hedy is an experienced cosmetic regulatory analyst in the ChemLinked team. She focuses on tracking, analyzing, and interpreting the latest cosmetic regulatory and market changes in China, Indonesia, Vietnam, and the rest of the Asia Pacific area. With an in-depth understanding of cosmetics regulations, she attended various industry conferences and presented several speeches in multiple industry conferences such as In-cosmetics Asia and often been interviewed by well-known cosmetics industry media. Area of expertise: China cosmetic import compliance, pre-market approval procedures, animal testing, Indonesia cosmetics halal certification, and Vietnam cosmetics compliance.