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  1. Abandoning Informed Consent.Robert M. Veatch - 1995 - Hastings Center Report 25 (2):5-12.
    Clinicians cannot obtain valid consent to treatment because they cannot guess which treatment option will serve a particular patient's best interests. These guesses could be made more accurately if patients were paired with providers who share their deep values.
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  • Shading the Truth in Seeking Informed Consent for Research Purposes.Sissela Bok - 1995 - Kennedy Institute of Ethics Journal 5 (1):1-17.
    I want to argue for two propositions. First, I suggest that what some researchers may take to be a simple trade-off between minor violations of the truth for the sake of access to far greater truths represents a profound miscalculation with far-reaching and cumulative reverberations. Second, I submit that today's research environment, as demanding, competitive, and sometimes bewildering as it is, offers genuine scope for what Murdoch calls truth-seeking, for imagining and questioning, and for relating to facts through both truth (...)
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  • (1 other version)Bioethics in argentina: A country report.Ruth Macklin & Florencia Luna - 1996 - Bioethics 10 (2):140-153.
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  • 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.
    The mission of the Indian Health Service affects what research is done and how It is reviewed and managed and in turn affects the forms and process used to obtain informed consent. Consent forms must be Informative and understandable to American Indian and Alaska Native potential volunteers; the process used to obtain informed consent must minimize any institutional pressure to participate. The IHS Institutional Review Boards developed seven research Model Volunteer Consent Forms.
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  • Collaborative Research Involving Human Subjects: A Survey of Researchers Using International Single Project Assurances.Alison Wichman, Janet Smith, Deloris Mills & Alan L. Sandler - 1997 - IRB: Ethics & Human Research 19 (1):1.
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  • The Institute of Medicine's Report on Women and Health Research: Implications for IRBs and the Research Community.Karen H. Rothenberg - 1996 - IRB: Ethics & Human Research 18 (2):1.
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  • (1 other version)Editorial: The "Best Proven Therapeutic Method" Standard in Clinical Trials in Technologically Developing Countries.Robert J. Levine - 1998 - IRB: Ethics & Human Research 20 (1):5.
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  • International Guidelines For Ethical Review Of Epidemiological Studies.[author unknown] - 1991 - Journal of Law, Medicine and Ethics 19 (3-4):247-258.
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