• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services


  • Print
  • Share
  • E-mail

Listeria monocytogenes Risk Assessment and Risk Management: December 4, 2003 Meeting

Listeria monocytogenes Risk Assessment Main Page

Meeting Agenda & Presentations

December 4, 2003


8:00   Registration

Opening Remarks

Ms. Janice Oliver

Deputy Director, Center for Food Safety and Applied Nutrition

Food and Drug Administration


Listeria monocytogenes: The Burden of Illness and the Public Health Challenge

Dr. Robert Tauxe

Centers for Disease Control and Prevention


Risk Assessment: Approach and Structure

Dr. Richard Whiting

Food and Drug Administration


Risk Assessment: Results and Conclusions

Dr. Robert Buchanan

Food and Drug Administration

10:45   --------BREAK--------

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--------

FDA/CDC Risk Management Action Plan

Dr. John Kvenberg

Food and Drug Administration


FSIS Risk Management Plan

Dr. Daniel Engeljohn

U.S. Department of Agriculture, Food Safety & Inspection Service

2:30   ---------BREAK--------

Questions for Risk Management Panel

MODERATOR: Dr. John Kvenberg (FDA)

Dr. Joe Baca (FDA)

Dr. Robert Brackett (FDA)

Ms. Majorie Davidson (FDA)

Dr. Daniel Engeljohn (FSIS)

Dr. Gary German (ORA)

Dr. Robert Tauxe (CDC)

Dr. Richard Whiting (FDA)

3:45 - 5:00   Public Comments