Legal analysis: responsible for the safety supervision and management of drugs, medical devices and cosmetics. To formulate supervision and management policies and plans, and organize the drafting of draft regulations; Responsible for the standardized management of drugs, medical devices and cosmetics. Organize the formulation and publication of national pharmacopoeia and other standards for drugs and medical devices, and participate in the formulation of the national basic drug list; Responsible for the registration management of drugs, medical devices and cosmetics, and formulate the registration management system; Responsible for the quality management of drugs, medical devices and cosmetics, and formulate and develop quality management standards; Responsible for the post-marketing risk management of drugs, medical devices and cosmetics, and organize the monitoring, evaluation and disposal of adverse drug reactions, medical device adverse events and cosmetic adverse reactions. To undertake the safety emergency management of drugs, medical devices and cosmetics according to law; Responsible for organizing and guiding the supervision and inspection of drugs, medical devices and cosmetics. Formulate an inspection system, investigate and deal with illegal acts in the registration of drugs, medical devices and cosmetics according to law, and organize and guide the investigation and handling of illegal acts in the production process according to responsibilities.
Legal basis: Drug Administration Law of People's Republic of China (PRC).
Article 6 The State implements the drug marketing license holder system for drug administration. The holder of the drug marketing license is responsible for the safety, effectiveness and quality controllability of the whole process of drug research and development, production, management and use according to law.
Article 7 In the research and development, production, marketing and use of drugs, laws, regulations, rules, standards and norms shall be observed to ensure the truthfulness, accuracy, completeness and traceability of the information in the whole process.
Article 8 The drug supervision and administration department of the State Council is in charge of drug supervision and administration throughout the country. The relevant departments of the State Council are responsible for drug supervision and administration within their respective functions and duties. The drug supervision and administration department of the State Council cooperates with the relevant departments of the State Council to implement the national drug industry development plan and industrial policy.