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Rules for Classification of Medical Devices

Provisions for Instructions and Labels of Medical Devices (Decree No.6 of China Food and Drug Administration)

NMPA issues the Guiding Principles for Capacity Building of Medical Device Inspection and Testing Organizations

NMPA issues the Rules for Unique Identification System for Medical Devices

Rules for Unique Device Identification System

Provisions for Unannounced Inspection of Drugs and Medical Devices (Decree No.14 of China Food and Drug

NMPA issues the Notice on Expanding the Pilot of the Medical Device Registrant System

Provisions for Medical Device Registration

NMPA issues the Announcement on the Requirements for Relevant Electronic Application Dossiers of Medical Devices

NMPA issues the Announcement on Medical Device GMP Appendix: Independent Software

NMPA issues the Announcement on the Requirements for Filing Review of Registration Items of Medical Device Products (Interim)

2018 Annual Report for Medical Device Registration released

NMPA issues Guidelines for Technical Review of the Registration of Synthetic Resin Teeth and Others

NMPA issues 27 medical device industry standards

NMPA issues the Announcement on Implementing Electronic Application of Medical Device Registration

NMPA issues the Announcement on Adjusting the Relevant Matters Concerning the Definition of the Attributes of Drug/Device Combination Products

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