Comparative Review of National Regulatory Frameworks in the Context of Secondary Use of Data for Research Across Europe

Olga Tzortzatou-Nanopoulou, Alexandra Ziaka, Carla Barbosa, Gauthier Chassang, Aliuska Duardo-Sánchez, Silja Elurnum, Christine Dalebø Gjerdevik, Radek Halouzka, Mette Hartlev, Ragnhild Angell Holst, Dorota Krekora Zając, Jan Kurán, Teodora Lalova-Spinks, Maria Luisa Lavitrano, Matteo Macilotti, Marina Makri, Signe Mežinska, Fruzsina Molnár-Gábor, Susanne Rebers, Jane ReichelSanta Slokenberga, Tom Southerington, Ruth Falzon

Publikation: Bidrag til bog/antologi/rapportBidrag til bog/antologiForskningpeer review

Abstract

Scientific research is a crucial tool for advancing healthcare and public health. In cross-border research collaborations, researchers need to navigate a complex pool of different requirements, which potentially hamper scientific research. This chapter aims to map the current legal landscape in seventeen Member States of the European Economic Area in the context of the secondary processing of health and genetic data for scientific research purposes. It critically assesses the transposition of GDPR in the national legal order of each State and its interplay with other applicable legislations. Our research findings show that only a handful examined Member States have a dedicated Act on secondary use, as the majority rely on provisions of different.
OriginalsprogEngelsk
TitelThe Discourse of Biorights : European Perspectives
RedaktørerJose-Antonio Seoane, Oscar Vergara
Antal sider27
Vol/bind109
UdgivelsesstedSwitzerland
ForlagSpringer Nature Switzerland
Publikationsdato2024
Sider243-269
Kapitel16
ISBN (Trykt)9783031668036
ISBN (Elektronisk)9783031668043
DOI
StatusUdgivet - 2024
NavnThe International Library of Bioethics
Vol/bind109
ISSN2662-9186

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