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  1. Consent for Data on Consent.Mollie Gerver - 2015 - Ethical Theory and Moral Practice 18 (4):799-816.
    There are instances where the provider of an intervention, such as surgery, has failed to obtain necessary informed consent from the recipient of the intervention. Perhaps the surgeon has failed to warn the patient that she may go into a coma, or even be killed, from the surgery. Sometimes, as a result of this intervention, the recipient cannot give informed consent to researchers for the release of their personal data precisely because of the intervention. If they are in a coma, (...)
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  • Protecting Patient Privacy Redux: Response to Open Peer Commentaries on “'You Don't Know Me, But …': Access to Patient Data and Subject Recruitment in Human Subjects Research”.Toby Schonfeld, Joseph S. Brown, N. Jean Amoura & Bruce Gordon - 2012 - American Journal of Bioethics 12 (1):W1 - W2.
    The American Journal of Bioethics, Volume 12, Issue 1, Page W1-W2, January 2012.
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  • The ASBH code of ethics and the limits of professional healthcare ethics consultations.Abraham Schwab - 2016 - Journal of Medical Ethics 42 (8):504-509.
    From the beginning, a code of ethics for bioethicists has been conceived of as part of a movement to professionalise the field. In advocating for such a code, Baker repeatedly identifies ‘having a code of ethics’ with ‘professionalization’. The American Society of Bioethics and Humanities (ASBH) echoes this view in their code of ethics for healthcare ethics consultants (HCECs)1 and the subsequent publication in the American Journal of Bioethics.2 Taking for granted that a code of ethics could be a valuable (...)
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