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From Vision to Certification: How MDT Achieved ISO Excellence

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Why the GDPR Code of Conduct Matters for CROs in a Global Data Privacy Landscape

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How Our ISO Certification Builds Trust Across the Life Sciences Ecosystem

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Europrivacy Certification Part II: Certification as a Tool for Transfers

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Life After Clinical Trial Closure: The Reality of Privacy Obligations Throughout the Archiving Period

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Europrivacy Certification Part I: Certification as a Data Protection Seal

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EDPB Guidelines 1/2026 on Scientific Research: a step forward for Life Sciences, but with tangible operational consequences

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Why APAC Is the Next Data Privacy Frontier for Life Sciences

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Can a DPO Trust AI for Legal Advice? We Tested Claude with a Legal Plugin

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European Health Data Space in Action: From Regulation to Real-World Implementation

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Privacy-Enhancing Technologies: Enabling Data Innovation Without Compromise

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Personal Data & Pseudonymization: What Changed in the Last 15 Months?

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Re-identification Risks and the Mosaic Effect : Are Health Data Ever Truly Anonymous ?

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European Biotech Act: Data Protection implications highlighted by EDPB-EDPS

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Enhancing compliance with the right to erasure: insights from EDPB’s 2025 coordinated enforcement action

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The UK New Complaints Requirement under the Data (Use and Access) Act 2025: What You Need to Know

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From Compliance to Confidence: Rethinking Health Data Governance

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Using AI for Legal Advice: Who is liable when the algorithm gets it wrong?

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Tokenization in Clinical Trial: linking Data while preserving Privacy

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Your Health Data in the Hands of Tech Giants: The Hidden Risks of Healthcare AI Agents

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Governing Data, Enabling Science: Lessons from 2025, Challenges for 2026

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When Is Data Really Anonymous? Lessons from EDPS v. SRB

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The make-or-break moment for EU Data Protection and for Life Science innovation.

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The European Biotech Act: A Turning Point We Are Excited About and Ready to Support

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