Protecting Vulnerable Research Subjects: Practical Realities of Institutional Review Board Review and Approval
Journal of Health Care Law and Policy 1998; 1(1): 88-104
Showing items related by title, author, creator and subject.
Protecting Research Participants Review of Institutional Review Boards: Management and Function, Edited by R.J. Amdur and E.A. Bankert; Institutional Review Board: Member Handbook, by R. Amdur; Study Guide for Institutional Review Board: Management and Function, by S. Kornetsky, A. Davis, and R.J. Amdur; Principles of Clinical Research, Edited by I. Di Giovanna and G. Hayes; Informed Consent in Medical Research, Edited by L. Doyal and J.S. Tobias; the Complete Guide to Informed Consent in Clinical Trials, Edited by T. Hartnett; Tuskegee's Truths: Rethinking the Tuskegee Syphilis Study, Edited by S.M. Reverby; European Neonatal Research: Consent, Ethics Committees and Law, Edited by S. Mason and C. Megone; the Ethics of Medical Research on Humans, by C. Foster; Ethical Issues in Biomedical Publication, Edited by A. Hudson Jones and F. McLellan; Fraud and Misconduct in Biomedical Research (3rd Edition), Edited by S. Lock, F. Wells, and M. Farthing; Biomedical Research Ethics: Updating International Guidel Nicholson, Richard (2002-11)
Unknown author (National Institutes of Health (United States). Office of Extramural Research. Office for Protection from Research Risks [OPPR], 1993)
Protecting Human Subjects in the NIH's Intramural Research Program: A Draft Instrument to Evaluate Convened Meetings of Its IRBs Wichman, Alison, Kalyan, Dev N.; Abbott, Lura J.; Wesley, Robert; Sandler, Alan L. (2006-05)