Wed, May 02
|FDA White Oak Bldg 32
RAPID Working Group Meeting
REGISTRY ASSESSMENT OF PERIPHERAL INTERVENTIONAL DEVICES (RAPID) WORKING GROUP MEETING
Time & Location
May 02, 2018, 7:00 AM
FDA White Oak Bldg 32, 10903 New Hampshire Ave, Silver Spring, MD 20993, USA
About the Event
Walk-in registrations are welcome day of the meeting.
Please click the links below to review select presentations from the meeting:
Jack Cronenwett, Dartmouth-Hitchcock / Society for Vascular Surgery
Pablo Morales, US Food and Drug Administration
Roseann White, Duke Clinical Research Institute
The SPEED OPG Results: First Public Look
Daniel Bertges, University of Vermont medical Center/Society for Vascular Surgery
RAPID SPEED Cost and Value to Industry: Key Features
Robert Thatcher, 4C Medical Technologies
Benefits of Industry Involvement
Melanie Raska, Boston Scientific
Intellectual Involvement and Buy-in: From UDI to Biostats
Ted Heise, MED Institute
Terrie Reed, US Food and Drug Administration
Supplemental UDI data for RAPID
Joseph Drozda, Mercy Health System
General core data elements for RAPID
James Tcheng, Duke University
NEST Coordinating Center Demonstration Project Status for RAPID: What does it mean?
Rachael Fleurence, National Evaluation System for health Technology Coordinating Center
ROI-Value Proposition for Registry Partners
Gregory Pappas, US Food and Drug Administration
Schuyler Jones, Duke Clinical Research Institute