EDPB Releases New 2026 DPIA Template for Public Consultation
The EDPB publishes a new 2026 DPIA template to standardise GDPR compliance. What it means for medical device manufacturers.
MedTech Europe Calls for Greater Alignment in EU Digital Omnibus Proposals
MedTech Europe highlights key challenges in the Digital Omnibus, including AI Act timelines, GDPR updates, and Data Act implications for manufacturers.
EU-U.S. Data Privacy Framework Updated: What It Means for Medical Device Manufacturers
New EU-U.S. Data Privacy Framework FAQ impacts data transfers to U.S. vendors. What this means for medical device manufacturers in 2026.