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

• 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)
• Physicians/informed Consent -- No Liability for Assault and Battery or Breach of Duty to Obtain Informed Consent Where Patient Voluntarily Executed Consent Document 

  Unknown author (1979-09)
• Informed Consent, Informed Refusal, Informed Choice -- What Is It That Makes a Patient's Medical Treatment Decisions Informed? 

  Ridley, Donald T. (2001)

  Informed consent is the fundamental ethical and legal doctrine that protects the patient's rights of personal autonomy and bodily self- determination. An adjunct to the doctrine of informed consent advanced by some is the ...