Responsibility in Investigations on Human Subjects
In: REPORT OF THE MEDICAL RESEARCH COUNCIL FOR 1962-1963 (Cmnd 2382), by the Medical Research Council. London: Medical Research Council, (Cmnd 2382), 1964. p. 21-25
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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 Unknown author (United States. Department of Health and Human Services.[HHS] Food and Drug Administration [FDA], 1981-01-27)