David Bourget (Western Ontario)
David Chalmers (ANU, NYU)
Rafael De Clercq
Jack Alan Reynolds
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Theoretical Medicine and Bioethics 27 (5):415-431 (2006)
In genomic research the ideal standard of free, informed, prior, and explicit consent is believed to restrict important research studies. For certain types of genomic research other forms of consent are therefore proposed which are ethically justified by an appeal to the common good. This notion is often used in a general sense and this forms a weak basis for the use of weaker forms of consent. Here we examine how the notion of the common good can be related to individual health, health care, and genomic research and we use this analysis to propose more precise criteria to justify forms of consent which diverge from the ideal standard.
|Keywords||Genomics genomic research informed consent public intersest common good|
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Citations of this work BETA
Margit Sutrop (2011). Changing Ethical Frameworks: From Individual Rights to the Common Good? Cambridge Quarterly of Healthcare Ethics 20 (04):533-545.
Luciana Caenazzo, Pamela Tozzo & Renzo Pegoraro (2013). Biobanking Research on Oncological Residual Material: A Framework Between the Rights of the Individual and the Interest of Society. [REVIEW] BMC Medical Ethics 14 (1):17.
Kadri Simm (2011). The Concepts of Common Good and Public Interest: From Plato to Biobanking. Cambridge Quarterly of Healthcare Ethics 20 (04):554-562.
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