Join Us at the FDA White Oak Campus or Via Livestream—No Fee for Registration

Patient-preference information (PPI) is increasingly being used in regulatory decision making for medical devices. This Summit will provide a forum to engage all stakeholders including patient representatives, medical device industry, researchers, payers and policymakers, healthcare providers, assessors, and regulators to discuss and explore the role, challenges, and opportunities of using patient-preference information across the healthcare ecosystem.

Jointly sponsored by ISPOR—the professional society for health economics and outcomes research—and the US Food and Drug Administration (FDA) Center for Devices and Radiological Health (CDRH), this Summit offers several avenues for engagement and learning…

Join Us In Person* - March 31, 2020
Attend the Summit in Person at the FDA White Oak Campus    
*Seating limited to 300 attendees. Registration for in-person event on first come, first served basis.

Register Online Now to Attend In-Person

Join Us Virtually - March 31, 2020
Attend the Summit via Livestream   


Pre-Event Webinar: “Patient Preference Information – What It Is and What It Is Not”** - March 4, 2020 at 12:00 Noon (EST)
**Open to all (including non-registrants) and optional for Summit attendees.

Register for Webinar Here



U.S. Food and Drug Administration (FDA)

Costs for this event were partially covered through unrestricted grants from the following organizations:
CVRx Inc., Edwards Lifesciences, and Evidation Health