Relevant tasks of the Central Procuratorate

1, responsible for national inspection and technical arbitration of pharmaceutical biological products and imported pharmaceutical biological products. 2, undertake the sampling work of national drugs, biological products and imported drugs and biological products, and provide technical data and analysis reports required by the national drug quality bulletin. 3 to undertake technical review, revision or drafting of national standards for drugs and biological products; To undertake the quality standards and related technical review of new drugs, biological products and imported drugs and biological products. 4 responsible for the development, standardization and distribution of certified reference materials for drugs and biological products, including national standard materials, standard materials, special reagents and medicinal materials. 5. Be responsible for the collection, identification, review, preservation and distribution of production strains, cell strains and medical standard strains. 6 to carry out scientific research related to the verification methods, quality, quality standards and reference materials of drugs and biological products, as well as the safety and effectiveness of drugs and biological products, and organize the formulation and implementation of the national drug inspection science and technology development plan. Assist the State Administration of Pharmaceutical Products in managing scientific and technological projects. 7. Guide the business and technical work of the Institute of Biological Products of the State Institute for Drug Control and the verification department of the production unit, help solve technical problems, and train technical and management personnel. 8 responsible for the organization of laboratory certification and the standardization and scientification of business management of drug inspection offices in provinces, autonomous regions and municipalities directly under the Central Government and port drug inspection offices. 9, comprehensive reporting and feedback of drug quality information. 10, responsible for the quality verification and quality standard audit of medical devices designated by the State Administration of Medical Supplies. 1 1. Carry out the verification of drugs and biological products and the standardization of experimental animals for research, and undertake the tasks of the National Rodent Seed Center and the National Laboratory Animal Quality Testing Center.