China Financial Daily

The Mainland’s imminent enactment of a new version of Good Manufacturing Practice
State Food and Drug Administration Commissioner of the Food and Drug inspectors MAO Zhen-Bin 27, held in Beijing the “Symposium improve the quality of drug production,” said China will soon enact new version of “Good Manufacturing Practice” (GMP), to ensure the quality and safety of national essential medicines the future production version of the national essential medicines need to refer to GMP standard.

MAO Zhen-Bin said that the state’s basic drug system is China’s health system reform in a new system, the State Food and Drug Administration have a high degree of attention to essential medicines will be prescribed, such as re-certification process, and requested to get GMP certification pharmaceutical enterprises in the production of essential drugs, must achieve a new version of GMP requirements. For some of the basic drug production than larger enterprises, in new factories and workshops in the process, they should consciously raise against the new standards.

GMP is a pharmaceutical manufacturing and quality management of basic criteria. In China in 1988 and formally promulgated the first pharmaceutical GMP, and in 1992 made the first amendment. In 1998 the establishment of the State Food and Drug Administration, immediately following the 1992 revised version of the GMP, and in August 1, 1999 came into effect, still used today.

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