Abstract
This chapter reviews the origin and development of bioethics in the United States and Canada, showing how the social and historical context created a specific, North American understanding of the rights of patients and research subjects. Bioethics, as practiced in the United States and Canada, privileges individual responsibility and autonomy over communal solidarity, and thus, it is at odds with bioethical framework described in the Universal Declaration on Bioethics and Human Rights. This disjuncture and the absence of specific recommendations for how to put the principles of the Declaration into practice locally have resulted in a limited awareness of the document in the region. Major actors in the North American bioethical community have not actively promoted the Declaration and it is rarely mentioned in the bioethics literature originating there. This situation suggests that, rather than setting a new agenda for the long-established bioethical community in North America, the Declaration will be more successful if it finds a way to become integrated into existing bioethical agendas.
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Kalousova, L., De Vries, R. (2014). North American Perspectives. In: ten Have, H., Gordijn, B. (eds) Handbook of Global Bioethics. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-2512-6_83
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DOI: https://doi.org/10.1007/978-94-007-2512-6_83
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