What drug safety credit files does the drug supervision and administration department establish?

The food and drug supervision and administration department shall establish the food safety credit files of the promoters, sellers and warehousing service providers in the centralized trading market within its administrative area, and truthfully record the results of daily supervision and inspection and the investigation and punishment of illegal acts. , and announced to the public in accordance with the law, real-time update. Increase the frequency of supervision and inspection of centralized trading market promoters, sellers and warehousing service providers with bad credit records; Relevant information about the promoters, sellers, warehousing service providers, their principal responsible persons and other directly responsible personnel of the centralized trading market with serious violations shall be classified as serious violations and published. The food and drug supervision and administration departments at the city and county levels shall gradually establish a pre-qualification credit commitment system for market sellers, and require sellers to make public commitments in a standardized format. If there is illegal and untrustworthy sales behavior, voluntarily accept credit punishment. Credit commitment shall be submitted to the seller's credit file, subject to social supervision, and serve as a reference for the management of post supervision.

Legal basis: Article 3 of the Drug Administration Law of People's Republic of China (PRC).

Drug management should focus on people's health, adhere to the principles of risk management, whole process control and social co-governance, establish a scientific and strict supervision and management system, comprehensively improve drug quality, and ensure drug safety, effectiveness and accessibility. Article 4 The state develops modern medicine and traditional medicine and gives full play to their roles in prevention, medical treatment and health care. The state protects wild medicinal resources and varieties of traditional Chinese medicine, and encourages the cultivation of genuine medicinal materials. Article 5 The State encourages the research and development of new drugs and protects the legitimate rights and interests of citizens, legal persons and other organizations in the research and development of new drugs. Article 6 The State implements the drug marketing license holder system for drug administration. The holder of the drug marketing license is responsible for the safety, effectiveness and quality controllability of the whole process of drug research and development, production, management and use according to law. 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.