Registration Open for Sept. 29 Webinar on New Edition of Registries Guide

Register now for a webinar on Sept. 29 from 2:30 to 3:30 p.m. ET to introduce AHRQ’s Registries for Evaluating Patient Outcomes: A User’s Guide, Fourth Edition. The online resource, also available as an e-book, provides best practices to guide registry design, operation, analysis and evaluation. Registries collect patient data to study various aspects of a disease, such as treatment patterns and variations in care. Registries may also assess treatment effectiveness, monitor safety and measure quality. The fourth edition of the user’s guide includes updates on registry planning, design, operations and analysis. It also provides guidance for addressing technical and cultural shifts in the clinical research environment since the first edition, including widespread use of electronic health record systems and the emergence of patient-centered outcomes research.