Blogs – Page 2 – RDPrivacy

RD Privacy Blog

Explore our featured blogs for insights, strategies, and updates on privacy, compliance, and data protection in the life sciences industry.

Pseudonymized Data in Clinical Trials: Why EDPB’s Perspective Should Prevail Over ICO’s Guidance

February 11, 2025

The European Data Protection Board (EDPB) Guidelines on Pseudonymization state: “Pseudonymised data, which could be attributed to a… Read More

Data Subject Rights in Clinical Trials

February 7, 2025

The General Data Protection Regulation (GDPR) grants individuals a range of rights over their personal data, and sponsors… Read More

When GDPR Gets Personal: Dutch DPA Holds Clearview AI Directors Accountable

January 23, 2025

In September 2024, the Dutch Data Protection Authority (DPA) made headlines by announcing an unprecedented move to hold… Read More

NOYB Qualified to Bring Collective Actions: Boost for GDPR Enforcement

December 9, 2024

In a significant development for data protection and privacy advocacy, noyb (None of Your Business), the European Center… Read More

How to Conduct a DPIA: Best Practices for Small Biopharma

December 2, 2024

Data Protection Impact Assessments (DPIAs) are essential tools for identifying and managing privacy risks, particularly when handling sensitive… Read More

HRA-Approved Privacy Language for Clinical Trial Consents

November 25, 2024

The Health Research Authority (HRA) in the UK has released updated, approved language for the privacy sections of… Read More

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