According to the query of relevant public information, GMP is an abbreviation of the English word GoodManufacturingPractices, which is written and formulated by six professors of the Temple University in the United States, and promulgated in the form of decrees by developed countries in Europe and the United States in the 60's and 70's of the twentieth century, which require pharmaceutical companies to widely adopt. It was first implemented in the United States in 1963.
Specification for Quality Management of Pharmaceutical Manufacturing (QMMP) stipulates that the basic requirements for pharmaceutical manufacturing management and quality control are designed to minimize the risk of contamination, cross-contamination, and mix-ups, errors, and other risks during the pharmaceutical manufacturing process, and to ensure that pharmaceuticals are consistently and stably produced to meet their intended use and registration requirements.
GMP is an acronym for GOOD MANUFACTURING PRACTICE, which means "Good Manufacturing Practice" in Chinese. The World Health Organization (WHO) defines GMP as the regulations that guide the production and quality management of food, drugs, and medical products.
GMP is a set of mandatory standards for pharmaceutical, food and other industries, requiring companies to meet the health and quality requirements from raw materials, personnel, facilities and equipment, production processes, packaging and transportation, quality control and other aspects of the relevant national regulations to form a set of operational practices to help companies improve the health of the corporate environment, timely detection of problems in the production process, to improve. Briefly, GMP requires pharmaceutical, food and other production enterprises should have good production equipment, reasonable production process, perfect quality management and strict testing system to ensure that the final product quality (including food safety and health) in line with regulatory requirements.
Legal basis:
Code of Practice for the Quality Management of Pharmaceutical Manufacturing of the People's Republic of China Article 3 This code, as part of the quality management system, is a basic requirement for the management and quality control of pharmaceutical production, and is designed to minimize the risk of contamination, cross-contamination, and confusion, errors and other risks in the process of pharmaceutical production, and to ensure the continuous and stable production of pharmaceuticals in accordance with the intended use and registration It is designed to minimize the risk of contamination, cross-contamination and mix-ups during the manufacturing process, and to ensure the consistent production of medicines for their intended use and registration.