Research Consent Forms and Animal Safety Data: A Case Study of Defensive Ethics
LoVerde, Mary E.
Prochazka, Allan V.
Byyny, Richard L.
Clinical Research. 1988 Oct; 36(6): 552-558.
Animal Experimentation; Comprehension; Consent Forms; Consent; Disclosure; Drug Industry; Drugs; Ethics; Food; Forms; Government; Government Regulation; Human Experimentation; Industry; Informed Consent; Investigators; Motivation; Paternalism; Patients; Regulation; Research; Research Ethics; Research Subjects; Risks and Benefits; Statistics; Toxicity; Volunteers;
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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)
Review by a Local Medical Research Ethics Committee of the Conduct of Approved Research Projects, by Examination of Patients' Case Notes, Consent Forms, and Research Records and by Interview Smith, Trevor; Moore, Edward J.; Tunstall-Pedoe, Hugh (1997-05-31)