CFDA put out the Quality management standard on the clinical trial of medical devices (Exposure Draft) for public comment
To further strengthen the management on the clinical trial of medical devices, comprehensively standardize the clinical trial of medical devices, ensure the rights and interests of subjects and improve the scientificalness of the clinical trial of medical devices, the China Food and Drug Administration (CFDA) formulated the Quality management standard on the clinical trial of medical devices (Exposure Draft) and put it out for public comment.
Information source: http://www.sda.gov.cn/WS01/CL0779/74610.html
