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Policies and Regulations
Revised Measures for Supervision and Administration of Medical Device Production and Measures for Supervision and Administration of Medical Device Operation are Issued and will Come into Force......
2022-03-23
Notice on Releasing the Guidelines for the Preparation of Product Technical Requirements for Medical Devices
2022-02-10
Notice of Nine Authorities on Issuing the Development Plan for the Pharmaceutical Industry during the 14th Five-Year Plan Period
2022-01-30
Notice on Matters Concerning the Implementation of the Class I Medical Device Product Catalog
2022-01-04
Interpretation of the Development Plan for the Medical Equipment Sector during the 14th Five-Year Plan Period
2021-12-28
The Meeting for Advancing Research on Regulatory System for Administration of Registration of Medical Devices is Held
2021-11-30
Interpretation of Classification Rules of In vitro Diagnostic reagents
2021-11-01
Announcement of State Drug Administration on the publication of the Regulations on Self-inspection Management for Medical Device Registration
2021-10-25
Announcement of the National Medical Products Administration on Matters Concerning the Implementation of Measures for the Administration of Registration and Filing of Medical Devices and Measures.....
2021-09-30
Announcement of the National Medical Products Administration, the National Health Commission and the National Healthcare Security Administration on the Unique Device Identification for the Second.....
2021-09-18
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