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NMPA Announcement on Including the Testing Methods for Azelaic Acid and Its Salts in Cosmetics and Other 5 Testing Methods into the Technical Specification for the Safety of Cosmetics (Edition 2015) (No. 45, 2024)
2025-02-19
The National Medical Products Administration (NMPA) has organized to formulate Testing Methods for Azelaic Acid and Its Salts in Cosmetics and other 5 testing methods, which have been reviewed and approved by the Chairman's Meeting of the NMPA's Cosmetic Standardization Technical Committee.
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NMPA Announcement on Provisions for Cosmetic Inspections (No. 52, 2024)
2024-04-29
To strengthen the supervision and administration and regulate cosmetic inspections, according to the Regulations on Supervision and Administration of Cosmetics, the Provisions for Registration and Notification of Cosmetics and the Provisions for Supervision and Administration of Cosmetic Manufacturing and Distribution, the NMPA formulated the Provisions for Cosmetic Inspections, which is hereby issued and will come into force from November 1, 2024.
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NMPA Announcement on Several Measures to Optimize the Management of Cosmetic Safety Assessment (No. 50, 2024)
2024-04-22
To further optimize the management of cosmetic safety assessment and orderly promote the implementation of the cosmetic safety assessment system, according to the Regulations on Supervision and Administration of Cosmetics, the Provisions for Registration and Notification of Cosmetics and the Technical Guidance for the Safety Evaluation of Cosmetics (2021 Edition) (hereinafter referred to as the Guidance) and other relevant regulatory requirements, the NMPA formulated Several Measures to Optimize the Management of Cosmetic Safety Assessment, which are hereby issued and will come into force from May 1, 2024.
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Announcement on Issuing the Guideline for the Collection and Reporting of Adverse Reactions to Cosmetics by Cosmetic Registrant and Filing Entity (Interim)
2024-04-19
To regulate and guide cosmetic registrants and filing entities to carry out the collection and reporting of adverse reactions to cosmetics, according to the Regulations on Supervision and Administration of Cosmetics, the Provisions for Supervision and Administration of Manufacturing and Marketing of Cosmetics, the Provisions for the Administration of Adverse Reaction Monitoring of Cosmetics and other relevant provisions, in accordance with the requirements of the National Medical Products Administration, the National Center for ADR Monitoring organized to formulate the Guideline for the Collection and Reporting of Adverse Reactions to Cosmetics by Cosmetic Registrant and Filing Entity (Interim), which is hereby issued.
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2023 National Popular Science Week for Cosmetic Safety Kicks Off in Beijing
2023-05-22
On May 22, the opening ceremony of the 2023 National Popular Science Week for Cosmetic Safety was held in Beijing.
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Provisions for Supervision and Administration of Manufacturing and Marketing of Cosmetics
2022-10-25
(Promulgated by Decree No. 46 of the State Administration for Market Regulation on August 2, 2021, these Provisions shall be effective as of January 1, 2022.)
