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Registry Assessment of Peripheral Interventional Devices (RAPID) Working Group Meeting

May 2 @ 07:00 - 16:00

Walk-in registrations are welcome day of the meeting.

Event Agenda

Register here

Please click the links below to review select presentations from the meeting:

RAPID SPEED: An Overview

Jack Cronenwett, Dartmouth-Hitchcock / Society for Vascular Surgery


Objectives of the Day

Pablo Morales, US Food and Drug Administration


Statistical Analysis Plan

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


Improving Access GUDID Data

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


Adding Data Sources

Schuyler Jones, Duke Clinical Research Institute


Details

Date:
May 2
Time:
07:00 - 16:00
Website:
https://duke.qualtrics.com/jfe/form/SV_bEEOdxH70vevrjn

Venue

FDA Headquarters, White Oak Campus
Silver Spring, MD 20993 United States + Google Map