Acceptance of Foreign Data and Institutional Review Boards (IRB) and Informed Consent Requirements
IRB INFORMATION SHEETS, January 1983. 6p.
Showing items related by title, author, creator and subject.
Guidance for Institutional Review Boards, Clinical Investigations, and Sponsors: Exception From Informed Consent Requirements for Emergency Research: Draft Guidance Unknown author (United States. Food and Drug Administration [FDA], 2006-07)
Draft Guidance for Institutional Review Boards, Clinical Investigators, and Sponsors; Exception From Informed Consent Requirements for Emergency Research: Notice Unknown author (United States. Food and Drug Administration [FDA], 2006-08-29)
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)