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Policies and Regulations
Announcement on Issuing the Good Vigilance Practice for MedicalDevices (Trial)
2026-04-23
Announcement on Issuing the Guidelines for Medical DeviceRegistrants to Conduct Risk Evaluation of Adverse Events (2026 Revision)
2026-04-22
Implementation Opinions of the National Medical ProductsAdministration on "AI Plus Drug Regulation"
2026-04-13
Notice on Matters Related to the Pre-review of Clinical TrialProtocols of Innovative Medical Devices
2026-04-09
Annual Report on Medical Device Standard Management in China (2025)
2026-03-10
2025 Annual Report on Medical Device Registration
2026-03-09
Decree of the State Council of the People's Republic of China
2026-02-10
Announcement of the National Medical Products Administrationon Issuing the Priority Review and Approval for the Catalogue ofHigh-end Medical Devices (2025 Edition)
2026-02-04
Announcement of the National Medical Products Administrationon Adjusting Some Contents of the Classification Catalogue forMedical Devices (No. 132, 2025)
2026-01-20
Announcement of the National Medical Products Administration on Issuing the Provisions on the Filing Administration of InternetDrug or Medical Device Information Services (No.123, 2025)
2026-01-06
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