When did GMP start in this country?

November 1975?

GMP is a set of mandatory standards applicable to the pharmaceutical, food and other industries, requiring enterprises to meet the health and quality requirements from raw materials, personnel, facilities and equipment, production process, packaging and transportation, quality control and other aspects in accordance with the relevant national regulations, to form a set of actionable operational norms to help enterprises to improve the corporate hygiene environment, and to identify problems in the production process in a timely manner, to improve.

According to Decree No. 79 of 2011 signed by the Minister of Health of the People's Republic of China, the "Good Manufacturing Practice (2010 Revision)" (hereinafter referred to as the new version of the GMP) has been considered and approved by the Ministerial Conference of the Ministry of Health on October 19, 2010, and will come into force on March 1, 2011 onwards.

Expanded Information:

GMP contains requirements for every aspect, from the factory building to the ground, the equipment, personnel and training, hygiene, air quality and safety. personnel and training, hygiene, air and water purification, production and documentation. It is an autonomous management system that focuses specifically on the implementation of product quality and health and safety in the manufacturing process.The elements set out in GMP are the minimum conditions that must be met by pharmaceutical processing companies.

GMP requires that manufacturers should have good production equipment, rational production process, perfect quality management and strict testing system to ensure that the quality of the final product (including food safety and hygiene) in line with regulatory requirements.

Baidu Encyclopedia-GMP