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  1. Rethinking research ethics.Rosamond Rhodes - 2005 - American Journal of Bioethics 5 (1):7 – 28.
    Contemporary research ethics policies started with reflection on the atrocities perpetrated upoconcentration camp inmates by Nazi doctors. Apparently, as a consequence of that experience, the policies that now guide human subject research focus on the protection of human subjects by making informed consent the centerpiece of regulatory attention. I take the choice of context for policy design, the initial prioritization of informed consent, and several associated conceptual missteps, to have set research ethics off in the wrong direction. The aim of (...)
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  • Does Research Ethics Rest on a Mistake? The Common Good, Reasonable Risk and Social Justice.Alex John London - 2005 - American Journal of Bioethics 5 (1):37 – 39.
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  • The Patient as Partner: A Theory of Human Experimentation Ethics.Robert Veatch - 1988 - Journal of Religious Ethics 16 (1):190-190.
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  • Adults Are Not Big Children: Examining Surrogate Consent to Research Using Adults with Dementia.Mark Yarborough - 2002 - Cambridge Quarterly of Healthcare Ethics 11 (2):160-168.
    Few early debates in bioethics invigorated the field to the same extent as the one concerning whether or not young children could be used in nontherapeutic research. Though some of the issues in the debate were never fully settled, a consensus emerged, reflected in the Common Rule—that surrogates could consent to use children in such research, although once the level of risk rises above minimal, additional stipulations are required. Nontherapeutic research on cognitively impaired elderly people raises equally complex ethical issues, (...)
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  • Rethinking Research Ethics.Rosamond Rhodes - 2010 - American Journal of Bioethics 10 (10):19-36.
    Contemporary research ethics policies started with reflection on the atrocities perpetrated upon concentration camp inmates by Nazi doctors. Apparently, as a consequence of that experience, the policies that now guide human subject research focus on the protection of human subjects by making informed consent the centerpiece of regulatory attention. I take the choice of context for policy design, the initial prioritization of informed consent, and several associated conceptual missteps, to have set research ethics off in the wrong direction. The aim (...)
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  • Deciding for Others at the End of Life: Storytelling and Moral Agency.Mark Yarborough - 2005 - Journal of Clinical Ethics 16 (2):127-143.
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