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药品的优劣是人命关天的大事,保障人民用药安全,首先要保证高效能、高质量的药品投放市场.药品生产及质量管理规范(GMP)是药品生产和质量保障的最好管理办法.美国是世界上最早建立GMP制度的国家(1963年).现在世界上许多发达国家的药品生产相继采用了GMP的管理方法,世界卫生组织(WHO)亦明确倡仪,非GMP条件下生产的药品禁止出口,达不到GMP要求的制药企业则失去进入国际市场的可能性.日本制药企业实行GMP的历史也较早,积累的经验亦较丰富.我国的GMP已于今年7月正式颁布,相信我国的药品
The merits and demerits of medicine are the vital events of human life and guarantee the safety of people’s medication. First of all, we must ensure that high-quality and high-quality medicines are put on the market. The GMP is the best management method for drug production and quality assurance. The United States is the first country in the world to establish the GMP system (1963). Now many developed countries in the world have successively adopted the GMP management method in drug production. The World Health Organization (WHO) has also clearly advocated that non-GMP drugs Pharmaceutical companies that ban exports and fail to meet the requirements of the GMP will lose the possibility of entering the international market. The history of the GMP adoption by Japanese pharmaceutical companies is also earlier and their accumulated experience is also abundant. The GMP in China was officially promulgated in July this year and believed China’s drugs