EU Digital Omnibus Simplifies AI Act Obligations; Rhode Island Enacts AI Healthcare Laws
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EU Digital Omnibus Simplifies AI Act Obligations; Rhode Island Enacts AI Healthcare Laws
Regulation (EU) 2026/1744 streamlines EU AI Act compliance, while Rhode Island enacts three AI healthcare laws. Key updates for biotech and healthtech teams.
EDPB Anonymisation Guidelines 2026 and Clinical Trial Data: What Life Sciences Organisations Must Know
EDPB Guidelines 02/2026 on anonymisation set new standards for clinical trial data. Learn the three-criteria test, enforcement lessons and compliance steps. iliomad.
AI Triage, Biopharma Workbenches and Crumbling Data Bridges: iliomad Weekly Digest
NHS AI triage, Anthropic Claude Science, medical AI privacy risks, MHRA GxP guidance, EDPS ADM checklist and the EU-US data transfer threat explained.
Human Intervention in Automated Decision-Making: What the EDPS Checklist Means for Life Sciences
The EDPS checklist on human intervention in automated decision-making carries direct implications for GDPR clinical trials. Learn what effective oversight requires.
Informed Consent Form (ICF) and Ethnicity Data: Justification Requirements Under GDPR and MR-001
Ethics committees require scientific justification for ethnicity data in the ICF. Learn how GDPR Article 9, MR-001 and EU CTR 536/2014 apply to your clinical trial.
Health Data Under Pressure: US Legislative Shifts, AI Privacy Risks and EU Cloud Sovereignty Disputes | Weekly Digest
This week: a US health data broker bill, Supreme Court FTC ruling threatening EU-US data flows, AI membership inference risks, and French cloud sovereignty tensions.
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