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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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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
Culture

Celebrating researchers (and my dad) during National Cancer Research Month

  • Truveta staff
  • May 24, 2022
Estimated conceptions, COVID-19, and STI cases
ResearchResearch Insights

Exploring birth rates and STI diagnoses during periods of high COVID-19 rates

  • Truveta Research
  • May 23, 2022
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