December 4, 2003
| 8:00 | Registration |
| 8:30 | Opening Remarks
Ms. Janice Oliver Deputy Director, Center for Food Safety and Applied Nutrition Food and Drug Administration |
| 8:45 | Listeria monocytogenes: The Burden of Illness and the Public Health Challenge
Dr. Robert Tauxe Centers for Disease Control and Prevention |
| 9:15 | Risk Assessment: Approach and Structure
Dr. Richard Whiting Food and Drug Administration |
| 10:00 | Risk Assessment: Results and Conclusions
Dr. Robert Buchanan Food and Drug Administration |
| 10:45 | -------- BREAK -------- |
| 11:00 | Questions to Risk Assessment Panel MODERATOR: Dr. Robert Buchanan (FDA) Mr. John Bowers (FDA) Dr. Mary Brandt (FDA) Dr. Clark Carrington (FDA) Ms. Janell Kause (FSIS) Dr. Richard Raybourne (FDA) Dr. Richard Whiting (FDA) |
| 12:00 | -------- LUNCH -------- |
| 1:30 | FDA/CDC Risk Management Action Plan
Dr. John Kvenberg Food and Drug Administration |
| 2:00 | FSIS Risk Management Plan
Dr. Daniel Engeljohn U.S. Department of Agriculture, Food Safety & Inspection Service |
| 2:30 | -------- BREAK -------- |
| 2:45 | Questions for Risk Management Panel MODERATOR: Dr. John Kvenberg (FDA) Dr. Joe Baca (FDA) Dr. Robert Brackett (FDA) Ms. Marjorie Davidson (FDA) Dr. Daniel Engeljohn (FSIS) Dr. Gary German (ORA) Dr. Robert Tauxe (CDC) Dr. Richard Whiting (FDA) |
| 3:45 - 5:00 | Public Comments |