SERIES: Active Medical Product Surveillance Roundtables | Number 10 of 19 « Previous | Next »

Sep 7

Past Event

Brookings Roundtable on Active Medical Product Surveillance: Overview of FDA’s Sentinel Initiative

Event Materials

Audio

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Summary

It has been three years since FDA launched the Sentinel Initiative and, since then, FDA has made significant progress. On September 7, the Engelberg Center hosted the first of the three-part Sentinel Initiative 101 Webinar Series, “Overview of FDA’s Sentinel Initiative” to review ongoing activities and accomplishments. The roundtable featured a presentation from Dr. Judy Racoosin, Sentinel Initiative Scientific Lead, Office of Medical Policy, Center for Drug Evaluation and Research, U.S. Food and Drug Administration.

Dr. Racoosin’s presentation provided a high-level review of the Sentinel Initiative’s scope and achievements including:

  • FDA’s 3-year vision for the Sentinel Initiative
  • A brief overview of the role of the Mini-Sentinel pilot, the Observational Medical Outcomes Partnership, the Federal Partners Collaboration, and the Brookings Institution cooperative agreement
  • Next steps for the Sentinel Initiative

Subsequent webinars in this series will provide a more in-depth overview of these pilot activities.

Event Agenda

  • Welcome and Introduction

  • Overview of Sentinel Initiative

    • Judy Racoosin

      U.S. Food and Drug Administration

Details

September 7, 2011

10:00 AM - 11:00 AM EDT

The Brookings Institution

Live Webinar

1775 Massachusetts Ave., NW

Map

For More Information

Engelberg Center for Health Care Reform

202.797.4391

SERIES: Active Medical Product Surveillance Roundtables | Number 10