BESTAO Review - Policy Briefing on China’s Pharmacovigilance System

MED-Technical Guidelines for Real-world Data for Clinical Evaluation of Medical Devices (for Trial Implementation)

MED-(English Version) 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-Notice by CFDA, AQSIQ and CNCA on the Exemption of Compulsory Certification for Certain Medical Devices