在制药业中 ,质量政策是遵从现行ＧＭＰｓ的关键。ＩＳＯ90 0 0指南要求制定一些质量政策以保证行政管理部门建立质量管理系统。已依照ＩＳＯ 90 0 0指南制订了欧洲ＧＭＰｓ ,已经形成强调对质量管理的责任。美国ＧＭＰｓ(修订版 )最近也已被修改 ,并且它们也要求由行政管理部 In the pharmaceutical industry, quality policy is the key to complying with current GMPs. The ISO 90000 guidelines require the development of quality policies to ensure that administrative departments establish quality management systems. European GMPs have been developed in accordance with the ISO 90 0 guidelines and have formed an emphasis on the responsibility for quality management. U.S. GMPs (revised editions) have also been recently modified, and they also require