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-Interpretation on Measures for the Supervision and Administration of Online Sale of Medical Devices

MED-(English Version) CFDA Reg TG PACS technical review guidance for registration

MED-(Chinese Version) Announcement by CFDA on Approval and Issuing of 120 Recommending Medical Device Sector Standard Including YYT 0090-2014 Uterine Curette