1, in order to strengthen the supervision and management of medicines, to ensure the quality of medicines, to ensure the safety of human medicines, to safeguard people's health and the legitimate rights and interests of the use of medicines, the enactment of this law.
2, in the Chinese people's *** and the territory of the State engaged in the research and development of drugs, production, operation, use and supervision and management of units or individuals must comply with this Law.
3. The State develops modern and traditional medicines, giving full play to their role in prevention, medical treatment and health care. The State protects the resources of wild medicinal herbs and encourages the cultivation of Chinese medicinal herbs.
4. The State encourages the research and creation of new medicines, and protects the lawful rights and interests of citizens, legal persons and other organizations in the research and development of new medicines.
5. The Drug Administration under the State Council is in charge of national drug supervision and administration. The relevant departments of the State Council are responsible for drug-related supervision and management work within their respective areas of responsibility.
Provincial, autonomous regions, municipalities directly under the Central People's Government Drug Administration is responsible for the supervision and management of medicines in the administrative region. The relevant departments of the people's governments of the provinces, autonomous regions and municipalities directly under the Central Government are responsible for the supervision and management of drugs within their respective areas of responsibility.
The drug supervision and management department of the state council shall cooperate with the state council department in charge of economic synthesis, the implementation of the state formulated drug industry development planning and industrial policy.
6, the drug supervision and management department set up or determined by the drug testing organizations, undertake in accordance with the law to implement the drug approval and drug quality supervision and inspection of drug testing work required.
Expanded Information
To start a pharmaceutical production enterprises must have the following conditions:
1, with the qualification of pharmacy technicians, engineers and technical personnel and the corresponding skilled workers;
2, with its pharmaceutical production of plant, facilities and sanitation environment;
3, with the ability to produce pharmaceutical products;
3, with the production of pharmaceutical products and the production of pharmaceutical products.
3, with the production of drugs for quality management and quality inspection of institutions, personnel and the necessary equipment;
4, with the regulations to ensure the quality of drugs.
Opening a pharmaceutical business must have the following conditions:
1, with the qualification of pharmacy technicians;
2, with the operation of the drugs appropriate business premises, equipment, storage facilities, sanitation;
3, with the operation of the drugs appropriate quality management organization or personnel;
4.
Baidu Encyclopedia - Chinese People's **** and State Drug Administration Law