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APHA Scientific Session and Event Listing |
3088.1: Monday, November 06, 2006: 10:30 AM-12:00 PM | |||
Oral | |||
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In response to a growing concern with health risks posed by approved drugs, the IOM was asked by the Food and Drug Administration to form a panel of experts to study the U.S. drug safety system. Following an extensive review, the IOM panel released its report in Sept., 2006. This session will review the charge given to the IOM and the resulting recommendations made by its panel. The FDA perspective on the panel’s recommendations and the broader implications of the report on the agency and the U.S. drug safety system will also be discussed. | |||
Learning Objectives: Refer to the individual abstracts for learning objectives | |||
Steven K. Galson, MD, MPH Kathleen Stratton, PhD Sa Edlavitch, PhD Hugh Tilson, MD, DrPH | |||
The FDA Request to IOM - Steven Galson, MD, MPH | |||
IOM Report: Process and Recommendations - Kathleen Stratton, PhD | |||
FDA Perspective on the Findings and Recommendations - Steven Galson, MD, MPH | |||
Comments from the Practitioner - Hugh Tilson, MD, DrPH | |||
Discussion: Dr. Edlavitch, Panel, Audience | |||
See individual abstracts for presenting author's disclosure statement and author's information. | |||
Organized by: | APHA |
The 134th Annual Meeting & Exposition (November 4-8, 2006) of APHA