First published in 2007, the AHRQ publication “Registries for Evaluating Patient Outcomes: A User’s Guide” is among the most cited texts on the subject of patient registries. This well-respected reference handbook provides practical information on the design, operation, and analysis of patient registries. The handbook has been updated multiple times and is now on its 4th edition. Join Rich Gliklich, CEO and Michelle Leavy, Head of Healthcare Research and Policy at OM1 in this two-part webinar series exploring the newest edition of the User’s Guide, which combines updates to the fundamentals and addresses innovations in registry design, operation, and analysis.
Register separately for each webinar if you wish to attend both.
Part 1: What’s New? Updates to the Fundamentals and Exploring Innovations
Part 2: Understanding Quality and Updates to the Criteria