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Policies and Regulations
Notice on Adjusting Part of the Category of Medical Device Classification
2021-01-04
Circular on the National Medical Products Administration on Issuing the Guidelines for Medical Device Registrants to Conduct Adverse Event Risk Evaluations of Products
2020-11-30
Circular on Issuing the Technical Guidelines for Using Real-World Data for the Clinical Evaluations of Medical Devices (for Trial)
2020-11-26
Eight Authorities Call for Innovative Development of Regulation of Drugs and Medical Devices in the Guangdong-Hong Kong-Macao Greater Bay Area (with Policy Interpretations)
2020-11-26
Announcement on Pilot Application of Electronic Registration Certificate for Medical Devices
2020-10-19
Notice on Matters Relating to Production of Imported Medical Devices by Enterprises within the Territory of China
2020-09-27
2020 No. 38 Announcement on Adjustment and Release of Catalogue of Technologies Prohibited or Restricted from Export
2020-08-31
Notice on Publicly Soliciting Opinions for Catalogue of Industries for Encouraging Foreign Investment (2020 Edition) (Exposure Draft)
2020-08-04
Science Popularization Video of Medical Device UDI
2020-08-03
Notice on Adjusting the Plan for Allocation of Large Medical Equipment in 2018—2020
2020-08-03
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