论文部分内容阅读
为了提高中成药厂的生产技术水平和产品质量,实现“让国药走向世界”的愿望,中国药材公司于一九八六年十一月颁布了《中成药生产管理规范》,作为我国中药行业的GMP。本文就中成药厂推行并实施GMP的必要性及做法要求谈一些个人的认识和体会。一、中成药厂实施GMP的必要性目前,中成药生产仍旧沿袭传统的管理方式,对于成品的质量凭藉专人取样,按一定的标准来检验判断产品的质量。这种检验把关目前固然还十分必要,但我们也应看到这种检验方法和手段的局限
In order to improve the production technology and product quality of the Chinese patent medicine factory and realize the desire to “let Sinopharm to the world”, China National Herbal Medicine Company promulgated the “Production Management Practice of Chinese Medicine” in November 1986 as the Chinese medicine industry in China. GMP. This article talks about some individuals’ understanding and experience about the necessity and practice requirements for the implementation of GMP in the Chinese patent medicine factory. I. The necessity of implementing GMP in Chinese patent medicine plants At present, Chinese patent medicine production still follows the traditional management methods, and the quality of finished products is sampled by special personnel, and the quality of finished products is determined according to certain standards. It is of course still necessary to check this kind of inspection, but we should also see the limitations of this inspection method and method.