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  1. Principles of Biomedical Ethics: Marking Its Fortieth Anniversary.James Childress & Tom Beauchamp - 2019 - American Journal of Bioethics 19 (11):9-12.
    Volume 19, Issue 11, November 2019, Page 9-12.
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  • Why America accepted bioethics.Daniel Callahan - 1993 - Hastings Center Report 23 (6).
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  • Truth or consequences: The role of philosophers in policy-making.Dan W. Brock - 1987 - Ethics 97 (4):786-791.
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  • A Rich Bioethics: Public Policy, Biotechnology, and the Kass Council.Adam Briggle (ed.) - 2010 - University of Notre Dame Press.
    Several presidents have created bioethics councils to advise their administrations on the importance, meaning and possible implementation or regulation of rapidly developing biomedical technologies. From 2001 to 2005, the President's Council on Bioethics, created by President George W. Bush, was under the leadership of Leon Kass. The Kass Council, as it was known, undertook what Adam Briggle describes as a more rich understanding of its task than that of previous councils. The council sought to understand what it means to advance (...)
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  • Attitudes toward the Newly Dead.William May - 1973 - The Hastings Center Studies 1 (1):3.
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  • Race, Racism, and Structural Injustice: Equitable Allocation and Distribution of Vaccines for the COVID-19.Helene D. Gayle & James F. Childress - 2021 - American Journal of Bioethics 21 (3):4-7.
    Inequity has been a hallmark of the COVID-19 pandemic in the United States, especially in the sharply disproportionate impacts among people of color. Recent studies have confirmed that t...
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  • Playing God? Human Genetic Engineering and the Rationalization of Public Bioethical Debate.John Berkman, Stanley Hauerwas, Jeffrey Stout, Gilbert Meilaender, James F. Childress & John H. Evans - 2004 - Journal of the Society of Christian Ethics 24 (1):183-217.
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  • Reflections on the National Bioethics Advisory Commission and Models of Public Bioethics.James F. Childress - 2017 - Hastings Center Report 47 (S1):20-23.
    The National Bioethics Advisory Commission, of which I was a member, was established by a 1995 executive order that identified its “first priority” as “the protection of the rights and welfare of human research subjects.” Not surprisingly, then, most of NBAC's work focused on research involving human subjects or participants. A second priority concerned “issues in the management and use of genetics information, including but not limited to, human gene patenting.” NBAC's charter (in contrast to the executive order) listed this (...)
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  • Splicing Life.[author unknown] - 1982
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