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What are the important laws and regulations on drug administration in China?
1, Drug Administration Law of People's Republic of China (PRC)

The Drug Administration Law of People's Republic of China (PRC) focuses on drug supervision and management, and deeply discusses drug evaluation and quality inspection, medical device supervision and management, drug production and management, drug use and safety supervision and management, standardized management of hospital pharmacies, drug inspection management, and drug centralized bidding and procurement management, which has scientific guiding significance for medical and health undertakings and development.

1984 was adopted at the 7th meeting of the Standing Committee of the 6th NPC on September 20th, and shall be implemented as of July 20th, 1985. The current version is 2065438+ revised at the 14th meeting of the 12th the NPC Standing Committee on April 24th, 2005.

2065438+0818122 October, the revised draft of the Drug Administration Law was submitted to the National People's Congress Standing Committee (NPCSC) for deliberation, which will comprehensively increase the penalties for the production and sale of counterfeit drugs and inferior drugs.

2. People's Republic of China (PRC) Pharmacopoeia

China Pharmacopoeia (abbreviated as "Pharmacopoeia") is a book published by China Medical Science and Technology Press on June 5, 20 15, which was created by the State Pharmacopoeia Committee.

China Pharmacopoeia is published in four parts: one part contains medicinal materials and decoction pieces, vegetable oil and extracts, prescription preparations and single-flavor preparations; The second part includes chemicals, antibiotics, biochemical drugs and radioactive drugs; Three collections of biological products; Four general principles of collection and loading, including: general principles of preparations, inspection methods, guiding principles, general principles related to reference substances and test solutions, pharmaceutical excipients, etc.

3. Measures for the administration of toxic drugs for medical use

In order to strengthen the management of toxic drugs for medical use and prevent poisoning or fatal accidents, these measures are formulated in accordance with the provisions of the Drug Administration Law of People's Republic of China (PRC). 5438+0988+0 15 was adopted at the 25th executive meeting of the State Council on June 5438+ 10/5, and 1988 was promulgated and implemented in the State Council on February 27th.

4. Regulations on the Administration of Precursor Chemicals

This is a regulation on the management of precursor chemicals. The State Council, People's Republic of China (PRC) was promulgated on August 26th, 2005, and implemented in June, 2005 165438+ 10/. * * * There are eight chapters and forty-five articles.

According to article 15 of the State Council Decree No.653 "Decision of the State Council on Amending Some Administrative Regulations" published on July 29th, 20 14.

According to Decree No.666 of the State Council issued on February 6, 20 16, Article 46 of the Decision of the State Council on Amending Some Administrative Regulations is amended as:

According to Decree No.703 of the State Council "Decision of the State Council on Amending Some Administrative Regulations" published on September 8, 2065438, Article 6 was amended.

5. Regulations on the protection and management of wild medicinal resources

The Regulations on the Protection and Management of Wild Medicinal Resources is an administrative regulation for the protection and management of medicinal wild animal and plant resources in China. 198710/kloc-0 was promulgated in the State Council on October 30th, and shall come into force on June 5438+0987 12 1.

China is rich in wild medicinal resources, but the situation of indiscriminate mining and hunting is very serious.

In order to protect and rationally utilize wild medicinal resources, the Regulations on the Protection and Management of Wild Medicinal Resources stipulates the management principles of wild medicinal resources, the species of wild medicinal materials under special state protection, the rules for hunting and gathering wild medicinal materials, the establishment and management of wild medicinal materials reserves, the management and export of wild medicinal materials, the prices, grade standards, rewards and punishments, etc.

The regulation declares that the state shall implement the principle of combining protection with hunting for wild medicinal materials and create conditions for artificial cultivation.

Baidu Encyclopedia-Measures for the Administration of Toxic Drugs for Medical Use

Baidu Encyclopedia-China People's Pharmacopoeia

Baidu Encyclopedia-People's Republic of China (PRC) Drug Administration Law