Using Patient-Preference Information in Medical Device Regulatory Decisions: Benefit-Risk and Beyond
September 29, 2020
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.
The virtual Summit is 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).
View an ISPOR Educational Webinar on this topic: Patient-Preference Information – What It Is and What It Is Not
Costs for this event were partially covered through unrestricted grants from the following organizations:
CVRx Inc., Edwards Lifesciences, and Evidation Health