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NMPA to enhance drug regulation under revised rules — committed to a people-centered healthy policy and strengthen high-effect regulation
The revised Regulation aims to further encourage drug research and innovation, strengthen the whole life-cycle control of drugs and provide a solid legal guarantee for high-level drug safety and the high-quality development of the pharmaceutical industry.
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Revision and Release of the Good Manufacturing Practice for Medical Devices
On November 4, the National Medical Products Administration (NMPA) released the revised version of the Good Manufacturing Practice for Medical Devices (hereinafter referred to as the GMP). The new GMP for medical devices shall come into effect as of November 1, 2026.
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NMPA Announcement on Issuing the Opinions on Deepening the Reform of Cosmetics Regulation and Promoting High-Quality Industry Development
The release of the Opinions is an important measure by the NMPA to implement the strategic deployment of the Party Central Committee and the State Council on comprehensive deepening of reform and promoting high-quality development. It will better safeguard the people's demand for cosmetics and inject a strong impetus into the high-quality development of the cosmetics industry.
- Announcement of the National Medical Products Administration on Issuing the Administrative Provisions on Inspection and Export Certificate for Pharmaceutical Products Exported by Pharmaceutical Manufacturers([2025] No. 113)
- Policy Interpretation of the National Medical Products Administration on Issuing the Administrative Provisions on Inspection and Export Certificate for Pharmaceutical Products Exported by Pharmaceutical Manufacturers
- Announcement of the National Medical Products Administration on the Release of the Good Manufacturing Practice for Medical Devices ([2025] No. 107)
- Policy Interpretation of the National Medical Products Administration on Issuing the Administrative Provisions on Inspection and Export Certificate for Pharmaceutical Products Exported by Pharmaceutical Manufacturers
- Announcement of the National Medical Products Administration on Issuing the Administrative Provisions on Inspection and Export Certificate for Pharmaceutical Products Exported by Pharmaceutical Manufacturers([2025] No. 113)
- Revision and Release of the Good Manufacturing Practice for Medical Devices
