People's Republic of China (PRC) State Administration of Pharmaceutical Products is a national bureau managed by the State Administration of Market Supervision.
According to the Decision of the Central Committee on Deepening the Reform of the Party and State Institutions, the Plan for Deepening the Reform of the Party and State Institutions and the Plan for Institutional Reform in the State Council approved by the First Session of the 13th National People's Congress, the State Administration of Pharmaceutical Products was established.
Examples of the main responsibilities of the State Administration of Medical Products
(a) responsible for the safety supervision and management of drugs (including traditional Chinese medicine and ethnic medicine, the same below), medical devices and cosmetics. To formulate policies and plans for supervision and management, organize the drafting of draft regulations, formulate departmental rules and regulations, and supervise their implementation. To study and formulate management and service policies to encourage new technologies and products of drugs, medical devices and cosmetics.
(two) responsible for the management of drugs, medical devices and cosmetics standards. Organize the formulation and release of national pharmacopoeia and other standards for drugs and medical devices, organize the formulation of cosmetics standards, organize the formulation of classification management systems, and supervise the implementation. Participate in the formulation of the national essential drug list and cooperate with the implementation of the national essential drug system.
(three) responsible for the registration and management of drugs, medical devices and cosmetics. Formulate a registration management system, strictly approve the listing, improve the measures to facilitate the examination and approval services, and organize their implementation.
(four) responsible for the quality management of drugs, medical devices and cosmetics. Formulate and develop quality management standards and supervise their implementation. Formulate production quality management standards according to responsibilities and supervise their implementation. Formulate operation and use quality management standards and guide their implementation.
The above contents refer to Baidu Encyclopedia-State Administration of Pharmaceutical Products; Official website of the State Administration of Medical Products-Main responsibilities