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“Ethics and Clinical Research” Revisited: A Tribute to Henry K. Beecher
Hastings Center Report 23 (5):31-39 (1993)
Abstract
The doctrine of informed consent, borrowed from the law of torts, cannot be readily transplanted into therapeutic settings. The broader, as yet unrealized, idea of informed consent, which suggests that parties must make decisions jointly, should guide interactions between physicians and patients or investigators and subjects.My notes
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Citations of this work
Making Research Consent Forms Informative and Understandable: The Experience of the Indian Health Service.William L. Freeman - 1994 - Cambridge Quarterly of Healthcare Ethics 3 (4):510.
Surrogate Decision Making for Severely Cognitively Impaired Research Subjects: The Continuing Debate.Evan DeRenzo - 1994 - Cambridge Quarterly of Healthcare Ethics 3 (4):539.
Both Sides of the Coin: Randomization from the Perspectives of Physician-Investigators and Patient-Subjects.Eric D. Kodish, Kathleen A. Kassimatis & Tsiao Yi Yap - 2010 - Ethics and Behavior 20 (5):380-386.
Pharmaceutical patenting and the transformation of American medical ethics.Joseph M. Gabriel - 2016 - British Journal for the History of Science 49 (4):577-600.
Of ethics committees, protocols, and behaving ethically in the field: a case study of research with elderly residents in a nursing home.Irena Madjar & Isabel Higgins - 1996 - Nursing Inquiry 3 (3):130-137.
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