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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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News

Health system spotlight: Tina Esposito, VP, CHIO, Business Intelligence and Analytics, Advocate Health

  • Truveta staff
  • December 13, 2022
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The 10 days of Truveta

  • Truveta staff
  • December 12, 2022
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Truveta partners honored as Modern Healthcare’s 100 Most Influential

  • Truveta staff
  • December 7, 2022
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Culture

Meet the Truveta MDs: Raj Brar, MD

  • Truveta staff
  • December 2, 2022
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News

Health system spotlight: Eric Eskioğlu, MD, MBA, FAANS; EVP, Chief Medical & Scientific Officer at Novant Health

  • Truveta staff
  • November 28, 2022
Culture

Highlighting National Diabetes Awareness Month with Karim Dabbagh

  • Truveta staff
  • November 21, 2022
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NewsResearch

Truveta Research presents at the 150th Annual APHA

  • Truveta staff
  • November 18, 2022
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NewsTechnology

Truveta Studio + Truveta Research on LinkedIn Live

  • Truveta staff
  • November 17, 2022
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Culture

Truvetan spotlight: Jose Camilo, Software Engineer

  • Truveta staff
  • November 11, 2022
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