Clinical Study Reflections: Another View: Commentary on: “Raising Suspicions with the Food and Drug Administration: Detecting Misconduct”

Science and Engineering Ethics 16 (4):705-711 (2010)
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Abstract

Federal regulations are the minimum requirements for conducting clinical studies. Some innovation would improve the situation of many involved in these studies, including: study subjects, those who monitor studies, and clinical investigators as well as Institutional Review Boards. Respecting patient and whistle-blower input; appreciating research staff contributions; and implementing a systems and partnership approach would foster quality and advance clinical research

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10.1007/s11948-010-9235-1

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