What you are saying is: GMP is the abbreviation of GOOD MANUFACTURING PRACTICE in English, and its Chinese meaning is "good production practice". Does the World Health Organization define GMP as regulations that guide the production and quality management of food, drugs, and medical products?
How can this be different from the general norms/standards of an industry? What do you want to know?
GMP is a set of mandatory standards applicable to pharmaceutical, food and other industries. It requires enterprises to achieve hygienic quality in accordance with relevant national regulations in terms of raw materials, personnel, facilities and equipment, production processes, packaging and transportation, quality control, etc. requirements, and form a set of operable operating specifications to help enterprises improve the corporate sanitary environment, promptly discover problems existing in the production process, and improve them. Briefly speaking, GMP requires pharmaceutical, food and other manufacturing companies to have good production equipment, reasonable production processes, perfect quality management and strict testing systems to ensure that final product quality (including food safety and hygiene) meets regulatory requirements.
On July 11, 1995, the Ministry of Health of China issued Wei Yaofa (1995) No. 35 "Notice on Carrying out Drug GMP Certification Work." Pharmaceutical GMP certification is a system for the state to implement GMP supervision and inspection on pharmaceutical production enterprises (workshops) and drug varieties in accordance with the law and obtain approval. Although the international concept of drugs includes veterinary drugs, only a few countries such as China and Australia separate GMP for human drugs and GMP for veterinary drugs.
Drug GMP certification is carried out at the national and provincial levels. According to the provisions of the "Regulations on the Implementation of the Drug Administration Law of the People's Republic of China", the drug regulatory authorities of the people's governments at or above the provincial level shall comply with the "Drug Regulations". "Good Manufacturing Practices" and the implementation methods and steps stipulated by the drug regulatory department of the State Council, organize the certification of pharmaceutical manufacturers; if they comply with the "Good Manufacturing Practices", a certification certificate will be issued. Among them, the drug regulatory department of the State Council is responsible for the certification of pharmaceutical manufacturing enterprises that produce injections, radioactive drugs, and biological products specified by the drug regulatory department of the State Council.