The Food Safety Department of the Food and Drug Administration undertakes the supervision and management of food safety in the consumption link; Formulate and supervise the implementation of food safety management norms in the consumer field, undertake food safety investigation and monitoring in the consumer field, and release relevant information on food safety supervision in the consumer field; Undertake cosmetic safety evaluation according to law; To undertake the supervision and management of cosmetics hygiene.
Extended data
The duties of the State Food and Drug Administration of the United States are:
(a) to formulate policies, plans and supervise the implementation of the safety supervision and management of drugs, medical devices, cosmetics and consumer foods, and to participate in the drafting of relevant laws, regulations and departmental rules.
(two) responsible for food hygiene licensing and food safety supervision and management in the process of consumption.
(three) to formulate and supervise the implementation of food safety management norms in the field of consumption, to carry out investigation and monitoring of food safety in the field of consumption, and to release relevant information on food safety supervision in the field of consumption.
(four) responsible for cosmetics hygiene license, hygiene supervision and management and cosmetics examination and approval.
(five) responsible for the administrative supervision and technical supervision of drugs and medical devices, responsible for the development, production, circulation and use of drugs and medical devices, and supervise the implementation.
(VI) Be responsible for the registration, supervision and management of drugs and medical devices, formulate national standards for drugs and medical devices and supervise their implementation, organize the monitoring of adverse drug reactions and adverse events of medical devices, be responsible for the re-evaluation and elimination of drugs and medical devices, participate in the formulation of the national essential drug list, cooperate with relevant departments to implement the national essential drug system, and organize the implementation of the classified management system for prescription drugs and over-the-counter drugs. ?
(seven) responsible for formulating and organizing the implementation of the supervision and management norms of traditional Chinese medicine and ethnic medicine, formulating the quality standards of traditional Chinese medicine and ethnic medicine, organizing the formulation of the quality management norms of traditional Chinese medicine production and the processing norms of traditional Chinese medicine decoction pieces and supervising the implementation, and organizing the implementation of the protection system of traditional Chinese medicine varieties.
(eight) to supervise and manage the quality and safety of drugs and medical devices, supervise and manage radioactive drugs, narcotic drugs, toxic drugs and psychotropic drugs, and release information on the quality and safety of drugs and medical devices. ?
(nine) to investigate and deal with food safety violations and the consumption behavior of drugs, medical devices and cosmetics in research and development, production, circulation and use.
(ten) to guide the local food and drug supervision and management, China inspection and information construction.
(eleven) to formulate and improve the qualification access system for licensed pharmacists, and to guide and supervise the registration of licensed pharmacists.
(twelve) to carry out international exchanges and cooperation related to food and drug supervision and management.
(thirteen) to undertake other tasks assigned by the State Council and the Ministry of Health. The above is copied from China of the US Food and Drug Administration. To understand the responsibilities of food and drug administrations in various provinces and cities, please go to the corresponding China to inquire.
References:
China People's Congress Network: The main responsibilities, internal organs and staffing requirements of the State Administration of Pharmaceutical Products