Summary

We had the honour to see our latest article   titled "What US trial sponsors should know about the GDPR" published in BioPharma Dive. In this article, we discuss what the GDPR is and why it matters to Life Sciences company. We also show how iliomad Health Data can help companies maintain GDPR compliance.

Link to the article :

https://www.biopharmadive.com/spons/what-us-trial-sponsors-should-know-about-the-gdpr/654291/

Seamus Larroque

CDPO / CPIM / ISO 27005 Certified

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March 12, 2025
Clinical Trials
Biotech & Healthtech
Data Transfers
Regulations & Guidelines
Clinical Trial Sponsor

Navigating Privacy Requirements for Clinical Trials Across Jurisdictions: Focus on China

China’s data protection regulations play a crucial role in clinical trials, requiring sponsors and researchers to comply with multiple laws, including the PIPL, GCP-2020, and cross-border data transfer rules. Unlike other jurisdictions, China imposes strict consent requirements, risk assessments, and regulatory filings, making compliance a key factor when selecting trial locations and managing participant data.

October 14, 2024
Clinical Trials
Guideline

Analyzing the Similarities and Differences Between ICH-GCP and GDPR in Clinical Trials

ICH-GCP and GDPR are vital for clinical trials, setting standards for participant protection and data integrity, with distinct focuses and enforcement approaches.