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From page 61... ...
10:20 Break FDA Postmarket Surveillance 10:30 Monitoring Device Safety: CDRH's Current System and Vision for the Future Susan Gardner, Director of the Center for Devices and Radiological Health's (CDRH's) Office of Surveillance and Biometrics 61
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From page 62... ...
Maisel, Director, Medical Device Safety Institute 11:50 FDA Recall Data Study Ralph Hall, Distinguished Visiting Professor of Law, University of Minnesota Law School 12:30 PM Lunch Non-FDA Sources of Adverse Event Data 1:30 The National Cardiovascular Data Registries: Opportunities and Challenges in Postmarket Surveillance Frederick A Masoudi, MD, MSPH, Associate Professor of Medicine, Denver Health Medical Center & University of Colorado; Senior Medical Officer, National Cardiovascular Data Registries 2:00 The VA‑CART Program: Integration of Real‑Time Data Collection into the Process of Clinical Care Paul D
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From page 63... ...
· arry Kessler, Professor and Chair, Department of L Health Services, School of Public Health, University of Washington 5:30 Adjourn
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