Protection of Human Subjects; Informed Consent; Standards for Institutional Review Boards for Clinical Investigations; and Clinical Investigations Which May Be Reviewed Through Expedited Review Procedure
Federal Register 1981 January 27; 46(17): 8942-8979
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United States. Department of Health and Human Services.[HHS] Food and Drug Administration [FDA]
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Protection of Human Subjects; Informed Consent; Standards for Institutional Review Boards for Clinical Investigations. Proposed Rule Unknown author (United States. Food and Drug Administration, 1988-11-10)