MHRA Outlines Data Requirements to Support Regulatory Decision-Making
The MHRA has published a paper on regulatory-grade data, real-world data and the data infrastructure needed to support safety surveillance and regulatory decision-making.
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.