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-(English version) Announce on Adjustment and Improvement of Certification Catalog and Implementation Requirements

Bestao Translation: CNCA-00C-005: 2014 - Requirements for Factory Quality Assurance Ability

MED-(Chinese Version)Announcement by CFDA on the Approval and Issuing of 93 Medical Device Sector Standards Including YY 0053—2016 Hemodiaysis and Relevant Therapies - Haemodialysers, Haemodiafilters and Haemoconcentrators