The official website of the State Food and Drug Administration website: cfda.gov.cn.
Major responsibilities of the State Food and Drug Administration
(a) Responsible for drafting draft laws and regulations on the supervision and management of food (including food additives, health food, hereinafter the same) safety, pharmaceuticals (including traditional Chinese medicines, ethnic medicines, hereinafter the same), medical devices, cosmetic supervision and management, and the formulation of policy planning. Formulate departmental regulations, promote the establishment of the implementation of food safety enterprise main responsibility, the local people's government is responsible for the mechanism, the establishment of food and drug major information direct reporting system, and organizing the implementation and supervision and inspection, and strive to prevent regional and systemic food and drug safety risks.
(2) is responsible for developing the implementation of food administrative licensing and supervise the implementation. It establishes a mechanism for the investigation and management of hidden food safety problems, formulates annual plans for national food safety inspections, major rectification and management programs and organizes their implementation. It is responsible for establishing a unified system for publishing food safety information and announcing major food safety information. Participate in the development of food safety risk monitoring program, food safety standards, according to the food safety risk monitoring program to carry out food safety risk monitoring work.
(C) is responsible for organizing the development and publication of the national pharmacopoeia and other drugs and medical equipment standards, classification and management system and supervise the implementation. Responsible for the development of drugs and medical devices development, production, operation, use of quality management standards and supervise the implementation. Responsible for drug and medical device registration and supervision and inspection. Establish the monitoring system for adverse drug reactions and medical device adverse events, and carry out monitoring and disposal work. To formulate and improve the qualification access system for practicing pharmacists, and guide and supervise the registration of practicing pharmacists. Participate in the formulation of the national essential drugs catalog and cooperate in the implementation of the national essential drugs system. To formulate methods for supervision and management of cosmetics and supervise their implementation.
(d) responsible for the development of food, drugs, medical devices, cosmetics supervision and management of inspection system and organize the implementation of the organization to investigate and deal with major violations. The establishment of problematic product recall and disposal system and supervise the implementation.
(E) is responsible for food and drug safety emergency response system, organization and guidance of food and drug safety emergency response and investigation and handling, supervision of the implementation of accident investigation and handling.
(F) is responsible for the development of food and drug safety science and technology development planning and organization and implementation, and promote food and drug inspection and testing system, electronic supervision and traceability system and information construction.
(VII) is responsible for carrying out food and drug safety publicity, education and training, international exchanges and cooperation. Promote the construction of integrity system.
(viii) to guide local food and drug supervision and management work, standardize administrative law enforcement behavior, and improve the administrative law enforcement and criminal justice convergence mechanism.
(ix) undertake the daily work of the State Council Food Safety Commission. Responsible for the comprehensive coordination of food safety supervision and management, and promote the improvement of coordination and linkage mechanism. Supervision and inspection of provincial people's governments to fulfill their responsibilities in food safety supervision and management, and is responsible for assessment and evaluation.
(J) undertake the State Council and the State Council Food Safety Commission assigned other matters.
Expanded:
Development of the People's Republic of China (PRC) and the State Food and Drug Administration (SDA):
The People's Republic of China (PRC) and the State Food and Drug Administration (SDA) department will be the responsibility of the Office of Food Safety, the Food and Drug Administration (FDA), and the General Administration of Quality Supervision, Inspection and Quarantine (AQSIQ) of the supervision and management of the food safety in the production chain,
The State Food and Drug Administration of the People's Republic of China (SFDA) was formed by integrating the responsibilities of the Food and Drug Administration (FDA), the Food and Drug Administration (FDA), the General Administration of Quality Supervision, Inspection and Quarantine (AQSIQ), and the General Administration of Industry and Commerce (AIC), and is responsible for supervising and administering the safety of medicines, medical devices, cosmetics, and food safety for consumption.
Chinese People's **** and the State Food and Drug Administration (CFDA) Generally refers to the State Food and Drug Administration (SFDA), an organization directly under the State Council. It is a drug supervision and management department set up by the national government, is part of China's drug administration supervision and management organization system, belongs to the national drug management organization system category.
Reference: State Food and Drug Administration - Official Website