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In the past few years, a handful of books have aimed to help members of institutional review boards (IRBs) fulfill their role of protecting those who participate in approved biomedical and behavioral studies. This book, the latest addition to the list, walks IRB members through the maze of ethical considerations, regulatory requirements, and procedural issues they must attend to during protocol review and their oversight and periodic reviews of approved studies. Mazur covers familiar terrain regarding the tasks of the IRB and the basic terms and concepts that members must understand, including attention to informed consent, the recruitment of research
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