药学英语药学英语 (37).pptVIP

Unit Twelve Good Manufacturing Practices (GMP) Part four 2. EU/UK GMP Requirements 欧盟/英国GMP要求 Two European directives lay down 制定 the principles and guidelines for GMP in the EU, one for medicinal products for human use and the other for veterinary [?vet?r?neri] 兽医的 products. These directives have been incorporated in the national Law of member states. The European Commission has issued nine volumes of the rules governing medicinal products in the EU. 欧盟GMP原则和指南包括两个指令，一个用于人用药物，另外一个用于兽药。 这些指令已经具体体现在各成员国的法律中。 欧盟委员会已经发布了九卷《欧盟医疗产品管理条例》。 The la