First published in 2007 as a reference handbook with practical information on the design, operation, and analysis of patient registries, the U.S. Agency for Healthcare Research and Quality’s (AHRQ) “Registries for Evaluating Patient Outcomes: A User’s Guide” is among the most cited texts on the subject of patient registries.

In September, the 4th edition of the handbook* will be released. Join AHRQ and Senior Editors of the User’s Guide for a webinar exploring what to expect and what’s new, including:

  • Using existing data sources and registries as sources for real-world data and real-world evidence for informed decision making
  • Using common data elements and standardized outcome measures
  • Effectively engaging different stakeholders, including patient representatives
  • Understanding evolving ethics, privacy, and informed consent requirements

Click here for additional information and registration details.

Related Content

Evidence Matters 2022

Evidence Matters 2022

Evidence Matters is a virtual one-day summit that brings the literature review community together from different industries to learn, engage, and solve ever-pressing evidence-based research challenges.