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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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Abby Stockwell with her husband in Philadelphia.
Culture

Truvetan spotlight: Abby Stockwell, Director of Product Marketing

  • Truveta staff
  • October 20, 2022
The Truveta team outside of HQ in Bellevue, Washington.
Culture

Truveta’s 4th Planning Week

  • Truveta staff
  • October 18, 2022
The HonorHealth logo
News

Welcome HonorHealth to Truveta

  • Truveta staff
  • October 17, 2022
The 1st Truveta Hackathon
Culture

Truveta celebrates first hackathon winners

  • Truveta staff
  • October 12, 2022
Truveta Research EHR data medical research public health
Culture

Meet Truveta Research

  • Truveta staff
  • October 11, 2022
LinkedIn Live intro with Terry Myerson, Lish Mark, and Ryan Ahern
News

LinkedIn Live highlights: Boston Scientific, PAD research, and health disparities

  • Truveta staff
  • October 5, 2022
A graph from the PAD insights.
ResearchResearch Insights

Digging deeper: Understanding more about patient subgroups with peripheral artery disease

  • Truveta Research
  • October 4, 2022
An image of Deb Nielsen, standing on a bridge.
Culture

The call that changed everything: Breast Cancer Awareness Month with Deb Nielsen

  • Truveta staff
  • October 3, 2022
Karina Davidson, SVP of Research at Northwell Health
News

Health system spotlight: Karina Davidson, SVP of Research and Dean of Academic Affairs at Northwell Health

  • Truveta staff
  • September 30, 2022
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