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我國臨床試驗倫理審查效率精進機制

Optimization of Ethics Review of Clinical Trials in Taiwan

摘要


本文針對我國過去及現今採取用以提升臨床試驗倫理審查效率之方式、程序及相關制度加以彙整,同時對實務現況所遇之困難進行分析,並進一步提出建議,以期藉由提升臨床試驗倫理審查程序之效率,落實受試者權益之保障,並提升臨床試驗之品質。

並列摘要


This is a review of process and practices in institutional ethics review of clinical trials in Taiwan, with a focus on items related to improving efficiency of the review process, especially for multi-center trials. Barriers to improving ethics review efficiency are identified and potential solutions are discussed. Better efficiency in ethics review of clinical trials will result in better protection of research subjects and higher overall quality of clinical trials.

參考文獻


蔡甫昌、姚智中、林志六、陳聰富、楊泮池:多中心臨床試驗聯合倫理審查機制之國際趨勢及台灣進展。台灣醫學2016;20:59-74。
The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use. Guideline for good clinical practice E6(r2) https://database.ich.org/sites/default/ files/E6_R2_Addendum.pdf/ Accessed August 12, 2021.
全國法規資料庫,藥品優良臨床試驗作業準則,2020年8月28日。https://law.moj.gov.tw/LawClass/LawAll.aspx?pcode=L0030056/ Accessed August 12, 2021.
法源法律網:醫療法施行細則,1987年8月7日。https://db-lawbank-com-tw.nthulib-oc.nthu.edu.tw/FLAW/FLAWDAT08.aspx?lsid=FL013536&ldate=19870807/ Accessed August 12, 2021.
法源法律網:醫療法施行細則歷史異動條文,2000年3月27日https://db-lawbank-com-tw.nthulib-oc.nthu.edu.tw/FLAW/FLAWDAT 08.aspx?lsid=FL013536&ldate=20000327&modify=1/ Accessed August 12, 2021.

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