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215 articles · page 1 of 18
The S-index is a proposed metric — the subject of a $1 million NIH prize competition — that would credit researchers for high-quality, reusable data…
The European Union (EU) Artificial Intelligence Act (Regulation (EU) 2024/1689) regulates AI by risk tier, and healthcare research organizations sit…
Article 89 of the General Data Protection Regulation (GDPR) is the provision that makes scientific research workable under European data protection…
The Gabriella Miller Kids First Data Resource Center (DRC) is a National Institutes of Health (NIH) Common Fund program that makes harmonized genomic…
A Sovereign AI deployment checklist gives procurement teams a structured way to verify that an AI platform for sensitive health data keeps that data…
Secondary use of health data means using health information for a purpose other than the one for which it was originally collected. Data recorded to…
Genomic data governance is the system of policies, roles, technical controls, and accountability mechanisms that determines how genomic data is…
Data residency requirements are legal or regulatory rules that determine where health data may be physically stored and processed — typically…
The European Health Data Space (EHDS) is a European Union regulation — Regulation (EU) 2025/327 — that creates a common legal framework for using…
Among electronic health record (EHR) vendors in 2026, the five most trusted by clinicians and informatics leaders are Epic , Oracle Health , MEDITECH…
Ministries of health choosing a Sovereign AI architecture face four practical options: hyperscaler-hosted national clouds, on-premise sovereign…
Government health programs evaluate Sovereign AI across three axes: architecture (federated compute where data never leaves the source), regulatory…
