Context-Relative Norms Determine the Appropriate Type of Consent in Clinical Biobanks: Towards a Potential Solution for the Discrepancy between the General Data Protection Regulation and the European Data Protection Board on Requirements for Consent

Clinical biobanks processing data of participants in the European Union (EU) fall under the scope of the General Data Protection Regulation (GDPR), which among others includes requirements for consent. These requirements are further specified by the Article 29 Working Party (WP29)—an EU advisory bod...

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Detalles Bibliográficos
Autores principales: Indrakusuma, R., Kalkman, S., Koelemay, M. J. W., Balm, R., Willems, D. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2020
Materias:
Original Research/Scholarship
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7755864/
https://www.ncbi.nlm.nih.gov/pubmed/33048326
http://dx.doi.org/10.1007/s11948-020-00271-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7755864/
https://www.ncbi.nlm.nih.gov/pubmed/33048326
http://dx.doi.org/10.1007/s11948-020-00271-9

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