The State Food and Drug Administration of the United States is directly affiliated to the State Council to comprehensively supervise the safety management and drug supervision of food, health products and cosmetics, and is responsible for the research, production, circulation and distribution of drugs (including Chinese herbal medicines, Chinese herbal pieces, Chinese patent medicines, chemical raw materials and their preparations, antibiotics, biochemical drugs, biological products, diagnostic drugs, radioactive drugs, narcotic drugs, toxic drugs, psychotropic drugs, medical devices, sanitary materials, medical packaging materials, etc.). ). Responsible for the comprehensive supervision, organization and coordination of food, health care products and cosmetics safety management, and organize the investigation and handling of major accidents according to law; Responsible for the examination and approval of health care products. The US Food and Drug Administration is a public institution, and there are also civil servants in public institutions.
What does the market supervision administration manage?
1. The management scope of the Market Supervision Administration is as follows:
(1) Responsible for comprehensive market supervision and management and intellectual property management;
(two) responsible for the unified registration of market entities;
(three) responsible for organizing and guiding the market supervision and comprehensive enforcement of intellectual property rights;
(four) responsible for the supervision and management of market order;
(5) Promote the implementation of competition policy as a whole and guide the implementation of fair competition review system.
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Legal basis: Drug Administration Law of People's Republic of China (PRC).
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.
The pharmaceutical supervisory and administrative departments of the people's governments of provinces, autonomous regions and municipalities directly under the Central Government shall be responsible for the pharmaceutical supervisory and administrative work within their respective administrative areas. The departments responsible for drug supervision and administration of the people's governments at the city or county level divided into districts (hereinafter referred to as drug supervision and administration departments) shall be responsible for drug supervision and administration within their respective administrative areas. The relevant departments of the local people's governments at or above the county level shall be responsible for drug supervision and administration within the scope of their respective duties.