DIMACS Working Group on Adverse Event/Disease Reporting, Surveillance, and Analysis IV

Fourth Meeting: February 10, 2006
DIMACS Center, CoRE Building, Rutgers University

Organizers:
David Madigan, Rutgers University, Statistics, madigan@stat.rutgers.edu
Presented under the auspices of the of the Special Focus on Computational and Mathematical Epidemiology.

DIMACS Working Group on Adverse Event/Disease Reporting, Surveillance, and Analysis I

DIMACS Subgroup on Adverse Event/Disease Reporting, Surveillance, and Analysis

DIMACS Working Group on Adverse Event/Disease Reporting, Surveillance, and Analysis II

DIMACS Working Group on Adverse Event/Disease Reporting, Surveillance, and Analysis III;
A DIMACS Panel at the Tenth Biennial CDC/ATSDR Symposium on Statistical Methods


Call for Participation:

This meeting is by invitation only.

Participants in the Working Group on Adverse Event/Disease Reporting, Surveillance, and Analysis IV
Robert Ball FDA
Warren Bilker University of Pennsylvania
John ClarkeGault Associates
Bill DuMouchel Lincoln Technologies
Susan Ellenberg University of Pennsylvania
Aimin Feng Rutgers Unviersity
Victor Gogolak Drug Logic
David Goldsmith Emory University
Manfred Hauben Pfizer
Guillermo Herrera CDC
Martin Kulldorff Harvard University
David Madigan Rutgers University
Lester Reich Pfizer
Henry Rolka CDC
Galit Shmueli University of Maryland
Ivan Zorych DIMACS


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Document last modified on February 9, 2006.