MED-(English Version) Quality Management Practice for Clinical Trials of Medical Devices

MED-(Chinese version) Announcements on Issues Related to the Extension of Registration and Application Materials for Medical Devices (Including In Vitro Diagnostic Reagents)

MED-(English version) Writing Specification for Periodic Risk Evaluation Report of Medical Devices

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