Informed Consent, Confidentiality, and Subject Rights in Clinical Trials
Proceedings of the American Thoracic Society 2007 May; 4(2): 189-193; discussion 193
Showing items related by title, author, creator and subject.
Competing Clinical Trials in the Same Institution: Ethical Issues in Subject Selection and Informed Consent Gordon, Elisa J.; Micetich, Kenneth C. (2002-03)
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)
A Unified Web-Based Query and Notification System (QNS) for Subject Management, Adverse Events, Regulatory, and IRB Components of Clinical Trials Mitchell, Rick; Shah, Maitri; Ahmad, Sushma; Rogers, Audrey Smith; Ellenberg, Jonas H. (2005)