欧洲药品管理局

欧洲药品管理局（）是一个欧盟药品评估机构。1995年至2004年这一段时间内，名為歐洲藥物檢驗局（）Set up by EC Regulation No. 2309/93 as the European Agency for the Evaluation of Medicinal Products, and renamed by EC Regulation No. 726/2004 to the European Medicines Agency, it had the acronym EMEA until December 2009. 。

欧洲药品管理局在欧洲的地位大致相当于美国食品药品监督管理局在美国的地位。

 参考 

延伸閱讀



 参见 




 EudraLex



 European and Developing Countries Clinical Trials Partnership
 European Clinical Research Infrastructures Network
 European Federation of Pharmaceutical Industries and Associations
 European Forum for Good Clinical Practice (EFGCP)
 ICH
 Inverse benefit law
 Medicines and Healthcare Products Regulatory Agency (MHRA, UK)
 Qualified Person
 Regulation of therapeutic goods
 Supplementary protection certificate (SPC)

 外部链接 


 药品临床应用委员会 (CHMP)
 兽医药品临床应用委员会 (CVMP)
 Heads of Medicines Agencies 
 Agencies of the European Union 
 The Rules Governing Medicinal Products in the European Union  (EudraLex)
 European Economic Area  (EEA)
 Health-EU Portal  official public health portal of the European Union

Category:歐洲聯盟公署
Category:1993年建立政府機構
Category:总部在荷兰的国际组织
Category:荷蘭醫療與健康組織
Category:阿姆斯特丹组织
Category:国家药品监管机构