• Base for Drug Clinical Trial,West China Hospital,Sichuan University,Chengdu 610041,China;
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药物上市前须经过人体试验,参与药物临床试验的受试者将承担不同程度的风险,我国GCP明确规定要充分保障受试者的权益,伦理委员会和知情同意书是保障受试者权益的主要措施,但在实际中仍存在不少问题。为此,如何切实保障受试者的权益,是临床试验所要解决的一个重要问题。

Citation: SHEN Qi,LIANG Derong,WU Songze. Few Wands of Subjects Protection,Rights and Benefits in Clinical Trials. West China Medical Journal, 2009, 24(2): 342-343. doi: Copy

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