David Bourget (Western Ontario)
David Chalmers (ANU, NYU)
Rafael De Clercq
Jack Alan Reynolds
Learn more about PhilPapers
Cambridge University Press (2007)
Informed consent is a central topic in contemporary biomedical ethics. Yet attempts to set defensible and feasible standards for consenting have led to persistent difficulties. In Rethinking Informed Consent in Bioethics Neil Manson and Onora O'Neill set debates about informed consent in medicine and research in a fresh light. They show why informed consent cannot be fully specific or fully explicit, and why more specific consent is not always ethically better. They argue that consent needs distinctive communicative transactions, by which other obligations, prohibitions, and rights can be waived or set aside in controlled and specific ways. Their book offers a coherent, wide-ranging and practical account of the role of consent in biomedicine which will be valuable to readers working in a range of areas in bioethics, medicine and law.
|Keywords||Informed consent (Medical law Bioethics Medicine Moral and ethical aspects|
|Categories||categorize this paper)|
|Buy the book||$16.47 used (59% off) $27.95 new (31% off) $39.99 direct from Amazon Amazon page|
|Call number||K3611.I5.M36 2007|
|ISBN(s)||0521874580 9780521874588 0521697476 9780521697477|
Setup an account with your affiliations in order to access resources via your University's proxy server
Configure custom proxy (use this if your affiliation does not provide a proxy)
|Through your library|
References found in this work BETA
No references found.
Citations of this work BETA
Nir Eyal & Neema Sofaer (2010). The Diverse Ethics of Translational Research. American Journal of Bioethics 10 (8):19-30.
Rebecca Erwin Wells & Ted J. Kaptchuk (2012). To Tell the Truth, the Whole Truth, May Do Patients Harm: The Problem of the Nocebo Effect for Informed Consent. American Journal of Bioethics 12 (3):22-29.
Nir Eyal (2014). Using Informed Consent to Save Trust. Journal of Medical Ethics 40 (7):437-444.
Deborah Zion, Linda Briskman & Bebe Loff (2010). Returning to History: The Ethics of Researching Asylum Seeker Health in Australia. American Journal of Bioethics 10 (2):48-56.
Emma C. Bullock (2014). Free Choice and Patient Best Interests. Health Care Analysis:1-19.
Similar books and articles
M. Sheehan (2011). Can Broad Consent Be Informed Consent? Public Health Ethics 4 (3):226-235.
Sheila McLean (2010). Autonomy, Consent and the Law. Routledge-Cavendish.
Deborah Bowman (2011). Informed Consent: A Primer for Clinical Practice. Cambridge University Press.
Jukka Varelius (2010). On Taylor's Justification of Medical Informed Consent. Bioethics 26 (4):207-214.
O. O'Neill (2001). Informed Consent and Genetic Information. Studies in History and Philosophy of Science Part C 32 (4):689-704.
Shaun D. Pattinson (2009). Consent and Informational Responsibility. Journal of Medical Ethics 35 (3):176-179.
David Shaw (2009). Prescribing Placebos Ethically: The Appeal of Negatively Informed Consent. Journal of Medical Ethics 35 (2):97-99.
Oonagh Corrigan (ed.) (2009). The Limits of Consent: A Socio-Ethical Approach to Human Subject Research in Medicine. Oxford University Press.
Michelle H. Biros (2007). Research Without Consent: Exception From and Waiver of Informed Consent in Resuscitation Research. Science and Engineering Ethics 13 (3):361-369.
Emma C. Bullock (2010). Informed Consent as Waiver: The Doctrine Rethought? Ethical Perspectives 17 (4):529-555.
Added to index2009-01-28
Total downloads114 ( #20,032 of 1,725,560 )
Recent downloads (6 months)6 ( #110,437 of 1,725,560 )
How can I increase my downloads?