Titlebook: Biobanks and Tissue Research; The Public, the Pati Christian Lenk,Judit Sándor,Bert Gordijn Book 2011 Springer Science+Business Media B.V.

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https://doi.org/10.1007/978-1-349-27722-3lies between the apparent necessity of obtaining informed consent from potential research subjects and the projected future use of the tissue. Specifically, under the doctrine of informed consent medical researchers are required to inform their potential research subjects about the relevant risks an

發(fā)展

https://doi.org/10.1057/9780230378629 of samples donors’ data have lately attracted much research work. The concern with privacy is particularly evident in the area of forensic uses of biobanks data. More concretely, opponents have argued that forensic data bases (i) discriminate against certain social groups, particularly when the dat

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https://doi.org/10.1007/978-1-349-20660-5the extent to which international regulation affects a basic notion of political realism: that States take action based upon their national interests. Before examining Irish and UK domestic regulation, it is necessary to discuss EU and COE regulation of research involving human tissue.