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Featured post

Regulatory-grade device evidence reimagined with new precision data

By linking unique device identifier (UDI) data with minute-level Admission–Discharge–Transfer (ADT), procedure logs, and chargemaster data, Truveta delivers the full picture of when, how, and in what context devices are used—accelerating regulatory submissions, health economics and outcomes research (HEOR), safety monitoring, and more.

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RWD RWE medical device research safety effectiveness HEOR EHR chargemaster unique device identifier ADT ICU procedure logs
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Partnering to improve data quality and health equity

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Unraveling Rare Diseases: Truveta's Impactful Research on Patient Populations - Explore real-time data insights for rare diseases research.
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Sharing our family’s journey in recognition of National Birth Defect Awareness Month

  • Truveta staff
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Health system spotlight: Angela Yochem, EVP Chief Transformation & Digital Officer, Novant Health

  • Truveta staff
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