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ISPOR-FDA Summit 2020

ISPOR-FDA Summit 2020

Tuesday, March 31, 2020 (7:30 AM - 4:30 PM) (EDT)

Description

ISPOR-FDA Summit 2020 

Themed: Using Patient-Preference Information in Medical Device Regulatory Decisions: Benefit-Risk and Beyond 

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

ISPOR and the US Food and Drug Administration (FDA) Center for Devices and Radiological Health (CDRH) will jointly sponsor a one-day Summit focusing on medical devices and the use of patient-preference information (PPI) in regulatory and other decision-making processes on March 31 at the FDA White Oak Campus in Silver Spring, MD, USA. 

Key Objectives for discussion at the Summit are:

 •To provide a forum for engaging 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 PPI. 

•To identify possible barriers and highlight the opportunities for integrating PPI throughout the product lifecycle. 

•To clarify the value of including PPI in regulatory, reimbursement, and patient-provider decision-making processes. 

Special Pre-Event ISPOR Educational Webinar: Patient Preference Information – What It Is and What It Is Not Webinar available on March 4, 2020 at 12:00 Noon (EST)* 

Details and register at www.ispor.org/Summit2020

FDA White Oak Campus

Silver Spring, MD United States
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