Guidance on Institutional Review Board Review of Clinical Trial Websites
Washington, DC: Office for Human Research Protections (OHRP), Department of Health and Human Services [HHS], 2005 September 20; 4 p. [Online]. Available: http://www.hhs.gov/ohrp/policy/clinicaltrials.html [2005 October 4]
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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)
Variation in Institutional Review Board Responses to a Standard Protocol for a Multicenter Clinical Trial Stair, Thomas O.; Reed, Caitlin R.; Radeos, Michael S.; Koski, Greg; Camargo, Carlos A. (2001-06)
Guidance for Industry: Institutional Review Board Review of Stand-Alone Health Insurance Portability and Accountability Act Authorizations; Availability Unknown author (United States. Food and Drug Administration [FDA], 2003-11-07)