Answer: D
The agency responsible for the management of medical device standards is the China Institute of Food and Drug Control; the agency responsible for the safety re-evaluation of drugs and medical devices is the National Medical Products Administration. The drug evaluation center of the regulatory department; the administrative matter acceptance service and complaint reporting center of the national drug regulatory department accepts complaints and reports of illegal activities; the organization that organizes the preparation and revision of the "Chinese Pharmacopoeia" and its supplements is the National Pharmacopoeia Commission.