Reporting of Informed Consent and Approval by Institutional Review Board (IRB) in Randomized Controlled Drug Trials Conducted in Nursing Homes (NH) From 1968 to 2004
Journal of the American Geriatrics Society 2007 April; 55(4, Supplement): S35-S36
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)
Ethical and Regulatory Challenges Associated With the Exception From Informed Consent Requirements for Emergency Research: From Experimental Design to Institutional Review Board Approval Vaslef, Steven N.; Cairns, Charles B.; Falletta, John M. (2006-10)