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《JournaloftheNationalCancerhstltute》1993年第85卷第15期报道了欧共体计划在1995年1月成立欧医药产品管理机构，负责协调新药的登记和监测产品的市场情况。从1995年开始欧洲的药品登记将采取两种途径。新的管理机构将掌握所有新的生物技术产品的集中审定，使12个欧共体国家
“Journal of the National Cancer STltute” Volume 85, Issue 15, 1993 Reported that the EC planned to set up the European Medicines Product Management Agency in January 1995 to coordinate the registration of new drugs and to monitor the product market. Drug registration in Europe from 1995 will take two approaches. The new regulatory body will have all the centralized validation of new biotech products, bringing 12 EU countries