What is the meaning of pharmaceutical affairs management

Definition of pharmaceutical affairs management: Pharmaceutical affairs management can be divided into narrow sense and broad sense.

The narrow sense of pharmaceutical affairs management refers to the supervision and management of drugs and related quality by the state in pharmaceutical activities.

That is to say, according to laws, administrative regulations and rules, the state supervises and manages the important links and administrative organization system in drugs and drug activities, that is, "strengthen the management of drug research, production, circulation, price, advertising and use according to law, strictly supervise quality, effectively guarantee the safety and effectiveness of people's drug use" and "safeguard people's health and legitimate rights and interests in drug use".

Generalized pharmaceutical affairs management refers to:

(1) State supervision and management over the quality of drugs and drug activities: The State conducts strict quality supervision over the research and development, production, circulation, price, advertising and use of drugs and drug activities.

(2) Macro-management of the industry when the state formulates the medical development plan.

(3) State supervision and management of medical devices, sanitary materials, pharmaceutical machinery and packaging materials.

④ Management of each subsystem's own operation and development in the pharmaceutical enterprise system.

2. The core of pharmaceutical affairs management: legal management of pharmaceutical activities.

3. The purpose of pharmaceutical affairs management: through the scientific, standardized and legal management of the activity process of each branch system of the pharmaceutical industry, to ensure the quality of drugs, ensure the safety and effectiveness of human medication, safeguard people's health and the legitimate rights and interests of medication, and promote the development of the pharmaceutical industry.