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dc.contributor.authorUrsin, Lars Øystein
dc.date.accessioned2015-01-29T15:00:32Z
dc.date.accessioned2016-07-11T13:30:24Z
dc.date.available2015-01-29T15:00:32Z
dc.date.available2016-07-11T13:30:24Z
dc.date.issued2009
dc.identifier.citationSolbakk, Jan Helge; Holm, Søren; Bjørn, Hofmann [Eds.] The Ethics of Research Biobanking p. 69-84, Springer, 2009nb_NO
dc.identifier.isbn978-0-387-93871-4
dc.identifier.urihttp://hdl.handle.net/11250/2396296
dc.description.abstractIn this chapter the notion of principled autonomy is presented, and the perspective enabled by this notion is applied in the field of biobanking. Some consequences of the perspective of principled autonomy on aspects of biobank recruitment are discussed in relation to concepts of voluntariness, consent, and privacy. These discussions aim to focus on the fruitfulness of the notion of principled autonomy in bringing out the interconnectedness of the duties and rights of biobank participants – both in general, and in a context of taking part in a research-based universal health care system in particular.nb_NO
dc.language.isoengnb_NO
dc.publisherSpringer USnb_NO
dc.titleDuties and Rights of Biobank Participants: Principled Autonomy, Consent, Voluntariness and Privacynb_NO
dc.typeChapternb_NO
dc.date.updated2015-01-29T15:00:32Z
dc.source.pagenumber69-84nb_NO
dc.identifier.doi10.1007/978-0-387-93872-1_6
dc.identifier.cristin42972
dc.description.localcodeThe original publication is available at http://link.springer.com/chapter/10.1007%2F978-0-387-93872-1_6nb_NO


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