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) Consultation Practice for Medical Device Technical Review

MED-Interpretation of Basic Requirements for Clinical Evaluation Data of In Vitro Diagnostic Reagents Exempt from Clinical Trials (for Trial Implementation)

MED-(English Version) Regulation on Supervision and Administration of Custom-made Medical Devices (Trial)