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835 articles · page 2 of 70
Implementing the Observational Medical Outcomes Partnership (OMOP) Common Data Model (CDM) means converting your source health data — electronic…
The European Union (EU) Artificial Intelligence Act (Regulation (EU) 2024/1689) regulates AI by risk tier, and healthcare research organizations sit…
An agentic federated Trusted Research Environment (TRE) is a research platform in which artificial intelligence (AI) agents carry out analytical work…
Clinical trial feasibility analysis with real-world data (RWD) means testing a protocol's eligibility criteria against actual patient records…
A federated Trusted Research Environment (TRE) reference architecture for a national genomics program keeps every genome and health record inside the…
Article 89 of the General Data Protection Regulation (GDPR) is the provision that makes scientific research workable under European data protection…
The FAIR data principles — Findable, Accessible, Interoperable, Reusable — are a set of fifteen guidelines, published by Wilkinson and colleagues in…
OMOP and FHIR solve different problems, and the honest answer to "which one?" is usually "both, in different places". Health Level Seven's Fast…
The Health Insurance Portability and Accountability Act (HIPAA) Privacy Rule recognizes exactly two ways to de-identify protected health information…
The Gabriella Miller Kids First Data Resource Center (DRC) is a National Institutes of Health (NIH) Common Fund program that makes harmonized genomic…
CFDE federated query refers to the ability, built by the United States National Institutes of Health (NIH) Common Fund Data Ecosystem (CFDE), to…
Biotech software is the set of specialized platforms that run the life-sciences value chain — from laboratory data capture and bioinformatics…
