#1303013: Public Workshop – Using Patient Preference Information in Medical Device Regulatory Decisions: Benefit-Risk and Beyond

BRI comment:	Registration required
Description:	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…
More info:	https://www.ispor.org/conferences-education/conferences/upcoming-conferences/ispor-fda-summit-2020

Date added	Feb. 18, 2020, 6:35 p.m.
Source	ispor
Subjects	Conferences and Seminars North America   HealthCare Industry News   U.S. Food and Drug Administration / FDA
Venue	The FDA’s White Oak Campus in Silver Spring, MD, March 31, 2020, midnight - March 31, 2020, midnight
Country	USA