MED-(English Version) Notice of the National Medical Products Administration on the Issuance of the Guidelines for Medical Device Registrants in Risk Evaluation of Product Adverse Events (No.78 in 2020)

MED-(English Version) Filing Review Requirements for the Registration of Change in Permitted Matter of Medical Devices (Trial)

MED-(English Version) Circular on Matters Concerning the Implementation of Unique Device Identification in First Batch of MD

Measures for the Administration of Radioactive Pharmaceuticals