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（）。

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
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参见
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• EudraLex

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• 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
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• [https://web.archive.org/web/20171115075355/http://www.ema.europa.eu/ema/index.jsp?curl=pages%2Fabout_us%2Fgeneral%2Fgeneral_content_000094.jsp&jsenabled=true 药品临床应用委员会] (CHMP)
• [https://web.archive.org/web/20171115082007/http://www.ema.europa.eu/ema/index.jsp?curl=pages%2Fabout_us%2Fgeneral%2Fgeneral_content_000262.jsp 兽医药品临床应用委员会] (CVMP)
• [http://www.hma.eu/ Heads of Medicines Agencies]
• [http://europa.eu/agencies/ Agencies of the European Union]
• [http://ec.europa.eu/health/documents/eudralex/index_en.htm The Rules Governing Medicinal Products in the European Union] (EudraLex)
• [http://ec.europa.eu/comm/external_relations/eea/ European Economic Area] (EEA)
• [http://ec.europa.eu/health-eu/index_en.htm Health-EU Portal] official public health portal of the European Union