In order to strengthen the supervision and management of medical device production, standardise the quality management of medical device production, according to the ‘supervision and management regulations of medical devices’ (State Council Decree No. 650), ‘supervision and management of the production of medical devices’ (State Food and Drug Administration Decree No. 7), the State Food and Drug Administration revised the ‘Code for the Quality Management of Medical Device Production’.

Medical Device ISO 14971 Risk Management Training Services.