Consent for Biobanking: The Legal Frameworks of Countries in the BioSHaRE-EU Project

Currently, there is no single, Europe-wide regulation of biomedical research using human samples and data. Instead, the law that applies spans a number of areas of law, such as data protection, clinical trials, and tissue regulation. In the absence of harmonized regulation, there is considerable scope for national legal variation. This article analyzes the legislative frameworks that apply to biobanking activities to identify differences in legal requirements between the BioSHaRE-EU project countries: Finland, France, Germany, the Netherlands, Norway, and the United Kingdom. This article highl... Mehr ...

Verfasser: Kaye, Jane
Briceño Moraia, Linda
Curren, Liam
Bell, Jessica
Mitchell, Colin
Soini, Sirpa
Hoppe, Nils
Øien, Morten
Rial-Sebbag, Emmanuelle
Dokumenttyp: status-type:publishedVersion
Erscheinungsdatum: 2016
Verlag/Hrsg.: New Rochelle
NY : Liebert
Schlagwörter: Article / biobanking / European Union / Finland / France / Germany / human / informed consent / landscape / law / legal procedure / legal service / medical research / Netherlands / Norway / priority journal / research ethics / United Kingdom / biobank / legislation and jurisprudence / organization and management / professional standard / Biological Specimen Banks / Biomedical Research / Consent Forms / Ethics Committees / Research / Humans / ddc:590 / ddc:610
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-29614225
Datenquelle: BASE; Originalkatalog
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Link(s) : https://www.repo.uni-hannover.de/handle/123456789/5386