Home> Laws and Regulations

NMPA Issued the Guidelines for the Verification of Medical Device Registration Quality Management System

CCFDIE|Updated: 2020-03-17

     

To strengthen the supervision and guidance over medical device product registration and further improve the quality of medical device registration QMS verification, NMPA has organized the formulation of and released on March 17, 2020 the Guidelines for Medical Device Registration Quality Management System Verification.