As real world data needs continue to grow, a new paradigm for patient registries is becoming increasingly important in
answering questions on treatment safety, effectiveness and value. These next generation registries leverage electronic health
records and other systems to reduce burden, increase enrollment and improve follow-up.
The latest edition of the Agency for Healthcare Research and Quality's Registries for Evaluating Patient Outcomes: A User's
Guide (scheduled for publication in August) helps bridge the gap between where registries have been and where they are
going.
This webinar will explore:
- Leveraging electronic health records and other systems in developing registries
- Using standardized outcome measures
- Building automated data networks to drive multi-stakeholder needs
- Leveraging advanced technologies for larger sample sizes and lower burden
- Harnessing unstructured data
Learning Objectives
- Understand new innovations and data quality criteria for registries
- Apply new technologies and approaches to RWD to registries

Speakers: 
Rich Gliklich, MD | CEO, OM1
Kathleen Troeger, MPH | Director of Outcomes Research at Hologic, Inc.
Michelle Levy, MPH |Head, Healthcare Research and Policy, OM1