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Andrew Garland

Bob Jones University
  •  Home
  •  Publications
    6
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    6

 More details
  • Bob Jones University
    School of Health Professions
    Assistant Professor
University of Virginia
Corcoran Department of Philosophy
PhD, 2020
CV
Homepage
Greenville, South Carolina, United States of America
0000-0001-8649-0976
Areas of Specialization
Meta-Ethics
Moral Epistemology
Biomedical Ethics
Moral Principles
History of Western Philosophy, Misc
Areas of Interest
Philosophy of Religion
Meta-Ethics
Normative Ethics
Social and Political Philosophy
17th/18th Century Philosophy
Moral Epistemology
Moral Principles
History of Western Philosophy, Misc
3 more
  • All publications (6)
  •  82
    Uncertain Bioethics: Moral Risk and Human Dignity, written by Stephen Napier
    Journal of Moral Philosophy 21 (1-2): 244-247. 2024.
    Biomedical Ethics
  •  76
    Personhood Is Still Useful, but Not for Everything
    American Journal of Bioethics 24 (1): 72-74. 2024.
    The concept of personhood has outlived its usefulness for bioethics, says Jennifer Blumenthal-Barby (2024). The concept of personhood has been important to the bioethics literature from fairly earl...
    Biomedical Ethics
  •  69
    Response to Open Peer Commentaries on “Do Clinicians Have a Duty to Participate in Pragmatic Clinical Trials?”
    with Stephanie Morain and Jeremy Sugarman
    American Journal of Bioethics 23 (10): 1-3. 2023.
    We very much appreciate the helpful and generous commentaries in response to “Do Clinicians have a Duty to Participate in Pragmatic Clinical Trials?” (Garland, Morain, and Sugarman 2023). In that a...
    Biomedical Ethics
  •  69
    Do Clinicians Have a Duty to Participate in Pragmatic Clinical Trials?
    with Stephanie Morain and Jeremy Sugarman
    American Journal of Bioethics 23 (8): 22-32. 2022.
    Clinicians have good moral and professional reasons to contribute to pragmatic clinical trials (PCTs). We argue that clinicians have a defeasible duty to participate in this research that takes place in usual care settings and does not involve substantive deviation from their ordinary care practices. However, a variety of countervailing reasons may excuse clinicians from this duty in particular cases. Yet because there is a moral default in favor of participating, clinicians who wish to opt out …Read more
    Clinicians have good moral and professional reasons to contribute to pragmatic clinical trials (PCTs). We argue that clinicians have a defeasible duty to participate in this research that takes place in usual care settings and does not involve substantive deviation from their ordinary care practices. However, a variety of countervailing reasons may excuse clinicians from this duty in particular cases. Yet because there is a moral default in favor of participating, clinicians who wish to opt out of this research must justify their refusal. Reasons to refuse include that the trial is badly designed in some way, that the trial activities will violate the clinician’s conscience, or that the trial will impose excessive burdens on the clinician.
    Medical Research Ethics
  •  115
    Toward Meeting the Obligation of Respect for Persons in Pragmatic Clinical Trials
    with Stephanie R. Morain, Stephanie A. Kraft, Benjamin S. Wilfond, Amy Mcguire, Neal W. Dickert, and Jeremy Sugarman
    Hastings Center Report 52 (3): 9-17. 2022.
    Hastings Center Report, Volume 52, Issue 3, Page 9-17, May–June 2022.
    Biomedical Ethics, MiscellaneousMedical Research Ethics
  •  62
    For the Common Good.Alex John London, 2021. New York, Oxford University Press. 480 pp, $99.00 (e‐book) (review)
    Journal of Applied Philosophy 39 (5): 935-937. 2022.
    Journal of Applied Philosophy, EarlyView.
    Applied Ethics
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