Showing items related by title, author, creator and subject.

• Variation Among Institutional Review Boards in Evaluating the Design of a Multicenter Randomized Trial 

  Stark, A R; Tyson, J E; Hibberd, P L (2010-03)

  OBJECTIVE: The objective of the study was to examine the variation among institutional review boards (IRBs) in evaluation of the study design of a multicenter trial. STUDY DESIGN: We assessed the first written response of ...
• Things Fall Apart. Can the Center Hold? Human Subjects Research Regulation and Participant Safety Review of Institutional Reveiw Boards: A Primer, by Teresa A. Williams, Richard G. Korman, Janet M. Lis and Melinda G. Murray; Evaluating The Science and Ethics of Research on Humans: A Guide for IRB Members, by Dennis J. Mazur; Clinical Research Law and Compliance Handbook, Edited by John E. Steiner; What the Doctor Didn't Say: The Hidden Truth About Medical Research, by Jerry Menikoff And Edward P. Richards 

  DeVille, Kenneth A. (2007-10)
• 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)