參考文獻
Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency.Official Journal of the European Union.47, Part 136
EUROPEAN MEDICINES AGENCY [EMA], The EMEA Code of Conduct (2006), http://www.ema.europa.eu/docs/en_GB/document_library/Other/2009/10/WC500004924.pdf (last visited Apr. 26, 2012)
EMA, European Medicines Agency policy on the handling of conflicts of interests of scientific committee members and experts (2012), http://www.ema.europa.eu/docs/en_GB/document_library/Other/2010/10/WC500097905.pdf (last visited Apr. 30, 2012).
EMA, Handling of conflicts of interest of the Management Board Public (2012), http://www.ema.europa.eu/docs/en_GB/document_library/Other/2012/04/WC500124975.pdf (last visited Apr. 30, 2012).
European expert list, EMA, http://www.ema.europa.eu/ema/index.jsp?curl=pages/about_us/landing/experts.jsp&mid=Wc0b01ac058043244a (last visited Apr. 26, 2012).
延伸閱讀
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- 李亞芝（2020）。組織變革與績效表現之關聯性分析－以歐洲製藥產業為例〔碩士論文，國立暨南國際大學〕。華藝線上圖書館。https://doi.org/10.6837/ncnu202000198
- 謝宗曄（2007）。歐洲聯盟消費者政策發展之研究-以商品安全為例〔碩士論文，淡江大學〕。華藝線上圖書館。https://www.airitilibrary.com/Article/Detail?DocID=U0002-1201200714115100
- 洪雯菊、林金定（2014）。歐盟罕病藥物供給、研發政策法規與藥品市場現況分析。身心障礙研究季刊，12(2)，67-76。https://www.airitilibrary.com/Article/Detail?DocID=17292832-201406-201412080001-201412080001-67-76
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