Research, experimentation, and clinical trials are, in most states, subject to a combination of federal and state
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Research, experimentation, and clinical trials are, in most states, subject to a combination of federal and state guidelines and regulations to ensure the proper supervision and control over research and experimentation involving human subjects. An institutional review board
(IRB) is responsible for reviewing, monitoring, and approving clinical investigations of drugs and medical devices that involve human subjects.
Written consent must be obtained from patients participating in clinical investigations.
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Related Book For
Legal Aspects Of Health Care Administration
ISBN: 9781284231526
14th Edition
Authors: George D. Pozgar
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