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What is the drug GMP?
The Good Manufacture Practice (GMP) is the basic guideline for the production and quality management of pharmaceuticals. It is suitable for the whole process of production of pharmaceutical preparations and the key processes affecting the quality of finished products in the production of APIs.
World Health Organization, 60 years began to organize the development of drugs GMP, in November 1975 officially announced GMP standards. China started from the 1980s and promulgated China's GMP in 1988, during which it was revised twice in 1992 and 1998. The Code for Quality Management of Pharmaceutical Production (Revised in 2010) was implemented on March 1, 2011.
GMP provides the content, food and drug processing enterprises must achieve the most basic conditions.
Veterinary drug GMP
The concept of international drugs, including veterinary drugs, only China and Australia and a few other countries is the drug GMP and veterinary drug GMP separated.
The Chinese veterinary drug industry GMP was implemented in the late 1980s. 1989, the Chinese Ministry of Agriculture issued a "veterinary drug production quality management practices (Trial)", in 1994 and issued a "veterinary drug production quality management practices (implementation)." From October 1, 1995 onwards, where the conditions of the pharmaceutical production enterprises (workshop) and pharmaceutical varieties, according to the application of drugs GMP certification. GMP certification certificate of the enterprise (workshop), in the application for the production of new drugs, the health administrative departments to give priority to accept. As of June 30, 1998, GMP certified enterprises (workshop), health administrative departments will no longer accept new drug production applications.

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