Toward a Tiered Approach to Consent in Biomedical Research
In: Árnason, Gardar; Salvör Nordal; Árnason, Vilhjálmur, eds. Blood & Data: Ethical, Legal and Social Aspects of Human Genetic Databases. Reykjavík: University of Iceland Press; 2004: 79-83.
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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)
Abramson, Norman S.; Meisel, Alan; Safar, Peter (1986-05-09)Federal regulations require researchers conducting clinical trials to obtain consent to experimentation from their intended subjects or, if the latter are incompetent, from next of kin. This requirement places constraints on ...