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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
Data
Technology
News & events
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
Culture

A backpack of rocks: My mental health journey

  • Truveta staff
  • May 19, 2022
News

Health system spotlight: Marcus Shipley, Senior Vice President & Chief Innovation and Information Officer, Trinity Health

  • Truveta staff
  • May 17, 2022
News

Truveta wins Health Innovation of the Year at 2022 GeekWire Awards

  • Truveta staff
  • May 13, 2022
News

Truveta featured on Changemakers Podcast from Microsoft

  • Truveta staff
  • May 10, 2022
Culture

Decisions made after I heard a snap

  • Terry Myerson, CEO
  • May 9, 2022
News

Truveta recognized by Fast Company’s World Changing Ideas 2022

  • Truveta staff
  • May 3, 2022
Culture

T is for Truveta…and team at Planning Week 3!

  • Lish Schilter
  • May 2, 2022
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