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Medical ethics / Science / Pharmaceutical industry / Design of experiments / Pharmacology / Informed consent / Clinical trial / Therapeutic misconception / Institutional review board / Clinical research / Ethics / Research


Attachment A: Approved by SACHRP July 20, 2011 Guidance on Applying the Regulatory Requirements for Research Consent Forms: What Should and Should Not be Included? Consent forms must convey basic elements of information
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Document Date: 2014-09-10 00:37:09


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