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Blog

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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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
Culture

Honoring my dad this Men’s Health Awareness Month

  • Truveta staff
  • June 13, 2022
Culture

Welcome 2022 Truveta interns!

  • Truveta staff
  • June 9, 2022
The Truveta team outside of HQ in Bellevue, Washington.
Culture

Why I work at Truveta

  • Truveta staff
  • June 3, 2022
Culture

Meet the Truveta MDs: Harshita Ravishankar, MD, MPA

  • Truveta staff
  • June 1, 2022
Technology

Truveta’s approach to protecting patient privacy

  • Truveta staff
  • May 31, 2022
Culture

Supporting Truvetans and mental health

  • Truveta staff
  • May 26, 2022
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