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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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Technology
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truveta
Technology

Building a learning public health system

  • Terry Myerson, CEO
  • June 20, 2023
Data

Alzheimer’s disease research: A new era

  • Truveta staff
  • June 15, 2023
ResearchResearch Insights

Ozempic, Wegovy, and Mounjaro: On- and off-label prescribing trends

  • Truveta Research
  • June 6, 2023
Truveta Language Model
Technology

A pragmatic suggestion for medical AI regulation

  • Terry Myerson, CEO
  • May 30, 2023
Data

Unlocking insights: Stroke research with Truveta

  • Truveta staff
  • May 25, 2023
A photo collage including a headshot photo of Dr. Marty Doerfler in the foreground with a team photo of Truveta employees in blue t-shirts in the background and a Truveta logo in the left corner.
Culture

Truveta spotlight: Dr. Marty Doerfler, EVP of Healthcare

  • Truveta staff
  • May 22, 2023
Technology

Q&A: Exploring with The Wall Street Journal Truveta’s EHR data on speech delays

  • Truveta staff
  • May 19, 2023
News

Truveta expands its community to more than 40 healthcare and life science organizations

  • Truveta staff
  • May 17, 2023
NewsResearch

Truveta collaboration with Harvard University researchers published in JAMA Network Open

  • Truveta Research
  • May 11, 2023
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