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Biobank research: who benefits from individual consent?
Requiring informed consent for research on stored tissue samples and associated data safeguards the autonomy rights of donors. But Joanna Stjernschantz Forsberg, Mats Hansson, and Stefan Eriksson argue that this policy not only defeats the interest of society but also runs counter to the interests o...
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Published in: | BMJ 2011-10, Vol.343 (7826), p.727-728 |
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description | Requiring informed consent for research on stored tissue samples and associated data safeguards the autonomy rights of donors. But Joanna Stjernschantz Forsberg, Mats Hansson, and Stefan Eriksson argue that this policy not only defeats the interest of society but also runs counter to the interests of the individuals it purports to protect |
doi_str_mv | 10.1136/bmj.d5647 |
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subjects | allmänintresse ANALYSIS Autonomy Bias Biobanker Biobanks Bioethics Bioetik Biological specimen banks Biological Specimen Banks - legislation & jurisprudence Ethics Genetic research Health care industry Human genetics Human Rights Humans Informed Consent informerat samtycke Medical ethics Medical research public good Public goods Regulation rättigheter Specimens Tissue samples Tissues |
title | Biobank research: who benefits from individual consent? |
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