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What inspections are the supervision and inspection of drug business activities divided into?
What inspections are the supervision and inspection of drug business activities divided into?

The supervision and inspection of drug business activities is an important means to ensure the safety of public drug use, which mainly includes licensing inspection, drug quality inspection, sales behavior inspection, after-sales service inspection, personnel training inspection, facilities and equipment inspection and sanitary conditions inspection.

Supervision and inspection of drug business activities is an important means to ensure the safety of public drug use. Through the inspection of the license, drug quality, sales behavior, after-sales service, personnel training, facilities and equipment, and sanitary conditions of pharmaceutical trading enterprises, we can find and correct existing problems in time, ensure the legal and compliant operation of pharmaceutical trading enterprises, and provide safe and effective drugs for the public. When conducting supervision and inspection, we should strictly follow the relevant laws, regulations and standards, and resolutely punish enterprises that do not meet the requirements to ensure the safety and health of the public.

To sum up, the supervision and inspection of drug business activities is an important means to ensure the safety of public drug use, which mainly includes licensing inspection, drug quality inspection, sales behavior inspection, after-sales service inspection, personnel training inspection, facilities and equipment inspection and sanitary conditions inspection. Through these inspection measures, the problems existing in pharmaceutical trading enterprises can be found and corrected in time, so as to ensure their legal and compliant operation and provide safe and effective drugs for the public.

Legal basis:

Article 7 of the Drug Administration Law of People's Republic of China (PRC): Engaged in drug research, production, marketing and use shall abide by laws, regulations, rules, standards and norms, and ensure that the information in the whole process is true, accurate, complete and traceable.

Article 8 of the Regulations for the Implementation of the Drug Administration Law of People's Republic of China (PRC): To establish a pharmaceutical production enterprise, it shall conform to the development plan and industrial policy of the pharmaceutical industry stipulated by the state, have the qualification of an enterprise as a legal person, and meet the following conditions: (1) It shall have qualified pharmaceutical technicians according to law; (2) Having a factory building, facilities and sanitary environment suitable for pharmaceutical production; (3) Having rules and regulations to ensure the quality of drugs; (4) Meet other conditions stipulated by the state.