Stay informed about the latest privacy developments in clinical research
RD PRIVACY BLOG
Privacy: The Next Competitive Edge in Clinical Operations
The Essential Role of the Data Protection Officer (DPO) in Clinical Trials
DPO clinical trials
ICO Fine Signals Urgency for GDPR in Clinical Trials
Running Trials in France? Know MR-001 & GDPR
Clinical Trial Agreements: Privacy Compliance Guide
Pseudonymized Data in Clinical Trials: Why EDPB's Perspective Should Prevail Over ICO's Guidance
Data Subject Rights in Clinical Trials
When GDPR Gets Personal: Dutch DPA Holds Clearview AI Directors Accountable
NOYB Qualified to Bring Collective Actions: Boost for GDPR Enforcement
How to Conduct a DPIA: Best Practices for Small Biopharma
HRA-Approved Privacy Language for Clinical Trial Consents
Why Non-EU Sponsors must sign Controller-Processor SCC’s with vendors in third-countries?
GDPR Compliance Guide: CRO Obligations Under EUCROF Code
UAE Clinical Trials: Progress, Privacy, & Global Standards
Third-Party Data Sharing in Clinical Trials: Navigating GDPR Compliance
GDPR Enforcement in Health Sector: Trends, Challenges & What's Next
The Hidden Risks of Genetic Data: A New Era of Discrimination?
GDPR and EU AI Act: Compliance Guide for the Healthcare Sector
Founder’s voice: Noyb vs Microsoft’s Xandr - Impact on Biopharma
