Listen to Webinar About the Newest User’s Guide, "Registries for Evaluating Patient Outcomes"
The AHRQ publication, "Registries for Evaluating Patient Outcomes: A User's Guide," is a reference handbook that provides best practices to guide design, operation, analysis, and evaluation of patient registries. In September 2020, AHRQ published the fourth edition of the handbook.
AHRQ and Senior Editors of the User's Guide hosted a 1-hour webinar to explore what's new in the fourth edition, including:
- Leveraging existing data sources and registries as sources for real-world data and real-world evidence.
- Using common data elements and standardized outcome measures; building effective governance policies and procedures.
- Understanding evolving ethics, privacy, and informed consent requirements.
