《药品生产质量管理规范》(GMP)是得到国际公认并为世界各国普遍采用的对药品生产全过程实施监督管理的法定技术规范。1998年,国家食品药品监督管理局组织对GMP进行修订,并于1999年8月1日施行。截止2004年6月底,全国38家疫苗生产企业均已陆续通过GMP认证检查,获得《药品GMP证书 The “Good Manufacturing Practices” (GMP) is internationally recognized and widely adopted by all the countries in the world to supervise the management of the entire process of producing pharmaceuticals. In 1998, the State Food and Drug Administration organized the revision of the GMP and came into effect on August 1, 1999. As of the end of June 2004, 38 vaccine manufacturers all over the country have successively passed the GMP certification inspection and obtained the "GMP Certificate of Drugs