Protection of Human Rights in Research Investigations (Letter and Response)
Bruya, Margaret Auld
AMERICAN REVIEW OF RESPIRATORY DISEASE 131(6): 966-967, June 1985
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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 creator (United States. Department of Health and Human Services.[HHS] Food and Drug Administration [FDA], 1981-01-27)
Catania, Joseph A.; Lo, Bernard; Wolf, Leslie E.; Dolcini, M. Margaret; Pollack, Lance M.; Barker, Judith C.; Wertlieb, Stacey; Henne, Jeff (2008-12)In a national survey of institutions with federally assured human research protection programs, we obtained workload and other relevant data on their Institutional Review Boards (IRBs) and management organizations. The ...