Journal of Medical Ethics 44 (6):392-396 (2018)

Authors
G. Owen Schaefer
National University of Singapore
Abstract
The predominant view is that a study using health data is observational research and should require individual consent unless it can be shown that gaining consent is impractical. But recent arguments have been made that citizens have an ethical obligation to share their health information for research purposes. In our view, this obligation is sufficient ground to expand the circumstances where secondary use research with identifiable health information is permitted without explicit subject consent. As such, for some studies the Institutional Review Board/Research Ethics Committee review process should not assess the practicality of gaining consent for data use. Instead the review process should focus on assessing the public good of the research, public engagement and transparency.
Keywords Research Ethics  Informed Consent  Health Data Research  Public Good
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DOI 10.1136/medethics-2017-104550
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References found in this work BETA

Scientific Research is a Moral Duty.J. Harris - 2005 - Journal of Medical Ethics 31 (4):242-248.
In Defense of the Duty to Participate in Biomedical Research.Rosamond Rhodes - 2008 - American Journal of Bioethics 8 (10):37 – 38.

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Citations of this work BETA

Precision Medicine, Data, and the Anthropology of Social Status.Hugh Desmond - 2021 - American Journal of Bioethics 21 (4):80-83.

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