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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
Research
Data
Technology
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Culture

Truveta spotlight: Tilak Paija Pun

  • Truveta staff
  • April 27, 2022
News

Earth Day 2022: Climate change is a health equity issue

  • Truveta staff
  • April 22, 2022
ResearchResearch Insights

Truveta insights: Do emergency department visits for asthma increase when the air quality index is high?

  • Truveta Research
  • April 22, 2022
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Culture

Health system spotlight: A conversation with Rod Hochman, Providence Health System

  • Truveta staff
  • April 20, 2022
Culture

Meet the Truveta MDs: Michael Simonov, MD

  • Truveta staff
  • April 12, 2022
ResearchResearch Insights

Truveta insights: The impact of Chadwick Boseman’s death on colonoscopy cancer screenings

  • Truveta Research
  • April 1, 2022
Culture

Truvetan spotlight: The making of Pradeep 2.0

  • Truveta staff
  • March 30, 2022
News

Truveta advances security and trust earning multiple ISO certifications, SOC 2 attestation

  • Truveta staff
  • March 30, 2022
Culture

Meet the Truveta MDs: Ryan Ahern, MD MPH

  • Truveta staff
  • March 22, 2022
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