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In Defense of Broad Consent
Cambridge Quarterly of Healthcare Ethics 21 (1):40-50 (2012)
Abstract
Proper procedures for informed consent are widely recognized as an ethical requirement for biomedical research involving human beings, in particular as a means to respect the autonomy and personal integrity of potential and actual research participantsMy notes
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Citations of this work
Broad consent for biobanks is best – provided it is also deep.Rasmus Bjerregaard Mikkelsen, Mickey Gjerris, Gunhild Waldemar & Peter Sandøe - 2019 - BMC Medical Ethics 20 (1):1-12.
Health Research with Big Data: Time for Systemic Oversight.Effy Vayena & Alessandro Blasimme - 2018 - Journal of Law, Medicine and Ethics 46 (1):119-129.
In Defence of informed consent for health record research - why arguments from ‘easy rescue’, ‘no harm’ and ‘consent bias’ fail.Thomas Ploug - 2020 - BMC Medical Ethics 21 (1):1-13.
Biomedical Big Data: New Models of Control Over Access, Use and Governance.Alessandro Blasimme & Effy Vayena - 2017 - Journal of Bioethical Inquiry 14 (4):501-513.
The biobank consent debate: Why ‘meta-consent’ is not the solution?Neil C. Manson - 2019 - Journal of Medical Ethics 45 (5):291-294.
References found in this work
Principles of biomedical ethics.Tom L. Beauchamp - 1979 - New York: Oxford University Press. Edited by James F. Childress.
Principles of Biomedical Ethics.Ezekiel J. Emanuel, Tom L. Beauchamp & James F. Childress - 1995 - Hastings Center Report 25 (4):37.
Broadening consent--and diluting ethics?B. Hofmann - 2009 - Journal of Medical Ethics 35 (2):125-129.
Coding and Consent: Moral Challenges of the Database Project in Iceland.Vilhjálmur Árnason - 2004 - Bioethics 18 (1):27-49.
Review of Ruth R. Faden and Tom L. Beauchamp: A History and Theory of Informed Consent. [REVIEW]William G. Bartholome - 1988 - Ethics 98 (3):605-606.
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