[U.S. Food and
Drug  Administration]

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The Clinical Impact of Adverse Event Reporting


Faculty

Dianne L. Kennedy, R.Ph., M.P.H.
Director, MEDWATCH
Office of the Commissioner, FDA

David J. Graham, M.D., M.P.H.
Acting Chief, Epidemiology Branch
Center for Drug Evaluation and Research, FDA

Thomas P. Gross, M.D., M.P.H.
Director, Division of Postmarket Surveillance
Center for Devices and Radiological Health, FDA

Richard M. Kapit, M.D.
Chief, Adverse Events Section, Epidemiology Branch
Center for Biologics Evaluation and Research, FDA

Lori A. Love, M.D., Ph.D.
Director, Clinical Research and Review Staff
Center for Food Safety and Applied Nutrition, FDA

Gale G. White, M.S., R.N.
Deputy Director, MEDWATCH
Office of the Commissioner, FDA

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