MED-Brief Introduction to the System for Submitting Periodic Risk Assessment Reports + Notice on the Launch of the Regular Risk Assessment Report Module of the National Medical Device Adverse Event Monitoring Information System

MED-(Bilingual) Decisions on cancellation for batch of administration approval matters

MED-(English version) Attach Supplementary and Correction Dossiers of Medical Device (sample form)

MED-(Bi) Notice of CFDA on Issuing the List of Medical Devices Exempted from Clinical Trials (Second Batch)