Informed Consent (I.C.) in Medical Research
Journal of Drug Research 1982 September; 7(6): 1409-1410
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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)
Informed Consent in Medical Research: Journals Should Not Publish Research to Which Patients Have Not Given Fully Informed Consent -- With Three Exceptions Doyal, Len (1997-04-12)Is the demand for informed consent absolute? In the first of this pair of articles a professor of medical ethics argues that the principle of informed consent to participate in medical research is fundamental if patients are ...
Suspension of Medical Research at West Los Angeles and Sepulveda Va Medical Facilities and Informed Consent and Patient Safety in Va Medical Research Unknown author (United States. Congress. House. Committee on Veteran's Affairs. Subcommittee on Oversight and InvestigationsSubscommittee on Health, 2000)