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98 articles · page 2 of 9
HL7 v2, CDA, and FHIR are three generations of Health Level Seven (HL7) standards for exchanging health information. HL7 v2 is a pipe-delimited…
Social determinants of health (SDOH) data describe the conditions in which people live, work, and age, such as income, education, housing, food…
External validation of a clinical AI model means testing it on data from sites, populations, or time periods that played no part in its development…
An external control arm is a comparison group built from patients outside the trial, usually drawn from real-world data such as electronic health…
You can train or adapt a foundation model on health data without centralizing it by sending the model to each data custodian, training locally inside…
The Global Alliance for Genomics and Health (GA4GH) standards are open technical specifications that let genomic and health data systems work…
Zero trust architecture for a Trusted Research Environment (TRE) means that no user, device, network, workload, or output is trusted by default, even…
Patient and public involvement (PPI) in Trusted Research Environment governance means giving patients and members of the public a formal, resourced…
Dynamic consent in biobanking is a digital, ongoing model of consent in which participants use a secure online interface to see how their samples and…
Health research metadata standards are shared vocabularies for describing datasets so that researchers can find them, judge whether they fit a study…
A computable phenotype is a precise, machine-executable definition of a clinical condition or characteristic, such as "adults with type 2 diabetes"…
Health data quality is measured by testing real-world data against defined dimensions, most commonly conformance, completeness, and plausibility, and…
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