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What does GSP mean?
GSP is the abbreviation of English Good Supply Practice, and it is called the quality management standard of pharmaceutical business in China.

GSP is a set of management procedures to control all factors that may cause quality accidents in the circulation of medical commodities, so as to prevent quality accidents. In the whole process of production, management and sales of medical commodities, quality problems may occur at any time due to internal and external factors, and strict measures must be taken in all these links to fundamentally ensure the quality of medical commodities.

The current GSP is a mandatory administrative regulation issued by the State Administration of Pharmaceutical Products, and it is the first GSP in China to be included in the legal scope.

Extended data:

Good supply specification

(20 12 and1.6 promulgated by Order No.20 of the former State Administration of Pharmaceutical Products on April 30, 2000, revised for the first time by the former ministerial meeting of the Ministry of Health, and revised for the second time by the executive meeting of China Food and Drug Administration according to 20.

Article 1 In order to strengthen the quality management of pharmaceutical trading, standardize pharmaceutical trading behaviors, and ensure the safety and effectiveness of human drug use, this Regulation is formulated in accordance with the Drug Administration Law of People's Republic of China (PRC) and the Implementation Regulations of the Drug Administration Law of People's Republic of China (PRC).

Article 2 This Code is the basic guideline for drug management and quality control.

Enterprises should take effective quality control measures in the procurement, storage, sales and transportation of drugs to ensure the quality of drugs, and establish a drug traceability system in accordance with relevant national requirements to realize drug traceability.

Article 3 Pharmaceutical trading enterprises shall strictly implement this Code.

Pharmaceutical production enterprises selling drugs and other drugs involved in storage and transportation in the process of drug circulation shall also meet the relevant requirements of this specification.

Article 4 Pharmaceutical trading enterprises shall adhere to honesty and trustworthiness and operate according to law. Any false or deceptive behavior is prohibited.

Reference source: Baidu Encyclopedia-Quality Management Standard for Drug Trading