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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
Research
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Technology
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Culture

Meet the Truveta MDs: Michael Wang, MD

  • Truveta staff
  • July 13, 2022
Cover of whitepaper: "Our approach to data quality" with Truveta branding
Technology

How we drive continuous improvement in our data quality

  • Truveta staff
  • July 7, 2022
An image of Debe Gash, SVP and Chief Digital Officer, Saint Luke's Health System
News

Health system spotlight: Debe Gash, SVP and Chief Digital Officer, Saint Luke’s Health System

  • Truveta staff
  • July 6, 2022
Cover image of data quality whitepaper
Technology

How we’re helping researchers navigate the imperfect world of real-world data

  • Truveta staff
  • June 29, 2022
Culture

“Never feel inferior” – A story of acceptance

  • Truveta staff
  • June 24, 2022
News

Collaboration announced between Truveta and Pfizer

  • Truveta staff
  • June 21, 2022
ResearchResearch Insights

Who are the people getting long COVID?

  • Truveta Research
  • June 21, 2022
Cover of whitepaper: "Our approach to data quality" with Truveta branding
Technology

How Truveta is delivering data quality at scale

  • Truveta staff
  • June 20, 2022
A few coworkers on the people team.
Culture

Take the Truveta office tour

  • Truveta staff
  • June 16, 2022
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