#1303013: Public Workshop – Using Patient Preference Information in Medical Device Regulatory Decisions: Benefit-Risk and Beyond
|BRI comment:||Registration required|
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…
|Date added||Feb. 18, 2020, 6:35 p.m.|
|Venue||The FDA’s White Oak Campus in Silver Spring, MD, March 31, 2020, midnight - March 31, 2020, midnight|