Wed, May 02 | FDA White Oak Bldg 32

RAPID Working Group Meeting

REGISTRY ASSESSMENT OF PERIPHERAL INTERVENTIONAL DEVICES (RAPID) WORKING GROUP MEETING
Registration is Closed

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.

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

Registration is Closed

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