MED-Guidelines for the Quality Control and Release of Finished Products of Medical Device

MED-(English Version) Explanation for CFDA Order 19[2016]_Naming Rules for Medical Devices

MED-(English Version) Filing Review Requirements for the Registration of Change in Permitted Matter of Medical Devices (Trial)

MED-Notice by Beijing Medical Products Administration on Issuing Beijing Municipal Discretion Benchmark for Administrative Punishment of Medical Device Supervision (for Trial Implementation)