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On October 4, the Engelberg Center for Health Care Reform hosted a roundtable webinar, "Conducting Real-Time Safety Evaluation with Medicare Data: Learnings from the SafeRx Project."Download presentation slides » (PDF)
The roundtable featured a presentation by Dr. Judy Racoosin of the Food and Drug Administration (FDA), who discussed a study conducted in the Medicare database that evaluated the impact of lags in claim processing and claim information updates (claims adjudication) on real-time evaluation of drug safety signals. This study was performed as part of the SafeRx project, a collaboration between FDA and the Centers for Medicare & Medicaid Services to utilize Medicare data for medical product active surveillance. Mini-Sentinel collaborators – including Dr. Jeff Brown of Harvard Medical School and Harvard Pilgrim Health Care Institute, and Dr. Jennifer Nelson of Group Health Research Institute and University of Washington School of Public Health – made additional comments regarding how the Mini-Sentinel Coordinating Center will evaluate similar issues in the Mini-Sentinel Distributed Dataset.
October 4, 2010
2:30 PM - 3:30 PM EDT
The Brookings Institution
Live Webinar
1775 Massachusetts Ave., NW
Washington, DC
Map
Engelberg Center for Health Care Reform engelbergevents [at] brookings.edu (202) 797-4391
Welcome and Introduction
Mark B. McClellan
Director
Economic Studies
View Bio
SafeRx Project Overview and Data Limitations
Judy Racoosin
Scientific Lead, Sentinel Initiative, Office of Medical Policy
Center for Drug Evaluation and Research, Food and Drug Administration
Remarks from Mini-Sentinel Collaborators
Jeff Brown
Assistant Professor, Department of Population Medicine, Harvard Medical School and Harvard Pilgrim Health Care Institute
Jennifer Nelson
Associate Investigator, Biostatistics Unit, Group Health Research Institute
Affiliate Assistant Professor, Biostatistics, School of Public Health, University of Washington
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