To strengthen medical device administration and standardize the sampling inspection of medical device quality, NMPA has organized the revision of and released on March 13, 2020 theAdministrative Measures for Sampling Inspection of Medical Device Quality. The Administrative Regulations on Quality Supervision and SamplingInspection of Medical Devices(CFDA Department of Medical Device Supervision [2013] No. 212) and theWork Procedures for National Medical Device Sampling Inspection(CFDA General Office [2014] No. 213) issued by the former China Food and Drug Administration shall be repealed simultaneously.
