The New EU-US Data Protection Framework’s Implications for Healthcare
Research output: Contribution to journal › Journal article › Research › peer-review
Standard
The New EU-US Data Protection Framework’s Implications for Healthcare. / Tschider, Charlotte; Corrales Compagnucci, Marcelo; Minssen, Timo.
In: Journal of Law and the Biosciences, 01.2024.Research output: Contribution to journal › Journal article › Research › peer-review
Harvard
APA
Vancouver
Author
Bibtex
}
RIS
TY - JOUR
T1 - The New EU-US Data Protection Framework’s Implications for Healthcare
AU - Tschider, Charlotte
AU - Corrales Compagnucci, Marcelo
AU - Minssen, Timo
PY - 2024/1
Y1 - 2024/1
N2 - In July 2023, the United States and European Union debuted the third iteration of cross-border agreements, the Data Protection Framework (DPF), designed to facilitate personal information transfer between the EU and the US. In healthcare, where cross-border healthcare and research initiatives are highly desirable and increasingly essential, this new framework could create new possibilities for streamlining the transfer of patient and research participant data. Although many DPF requirements may be familiar to US organizations required to comply with HIPAA, a failure to address health privacy requirements in individual EU countries or a lack of understanding where full General Data Protection Regulation (GDPR) compliance is actually needed may complicate compliance goals. In addition to outlining key DPF requirements, we offer alternatives that can improve the likelihood of reliable data transfer between the U.S. and EU and call on officials to consider the DPF’s impact for health and research organizations.
AB - In July 2023, the United States and European Union debuted the third iteration of cross-border agreements, the Data Protection Framework (DPF), designed to facilitate personal information transfer between the EU and the US. In healthcare, where cross-border healthcare and research initiatives are highly desirable and increasingly essential, this new framework could create new possibilities for streamlining the transfer of patient and research participant data. Although many DPF requirements may be familiar to US organizations required to comply with HIPAA, a failure to address health privacy requirements in individual EU countries or a lack of understanding where full General Data Protection Regulation (GDPR) compliance is actually needed may complicate compliance goals. In addition to outlining key DPF requirements, we offer alternatives that can improve the likelihood of reliable data transfer between the U.S. and EU and call on officials to consider the DPF’s impact for health and research organizations.
KW - Faculty of Law
KW - data protection
KW - data sharing
KW - collaboration
KW - medical research
KW - privacy
M3 - Journal article
JO - Journal of Law and the Biosciences
JF - Journal of Law and the Biosciences
SN - 2053-9711
ER -
ID: 374787779