This webinar is designed to help professionals in the field of Pharmacovigilance, Epidemiology and Medical Affairs understand how they can harness the power of active safety surveillance for themselves.
TORONTO (PRWEB)
October 28, 2020
Current safety management practices are largely centered on the review and analysis of spontaneous adverse events reported by healthcare professionals, caregivers and patients. While existing processes have been instrumental in identifying new and unsuspected safety concerns in the past, the availability of longitudinal real world data and modern digital technologies offers a new paradigm for enhancing drug safety knowledge. Through the Sentinel Initiative, the FDA has built a robust system for gleaning intelligence from real world data. The FDA is now actively using Sentinel, and the Active Risk Identification and Analysis (ARIA) system, to review safety concerns for several drugs.
This webinar is designed to help professionals in the field of Pharmacovigilance, Epidemiology and Medical Affairs understand how they can harness the power of active safety surveillance for themselves.
Join Dr. Judith Maro, PhD, Assistant Professor in the Department of Population Medicine, Harvard Medical School and the Harvard Pilgrim Health Care Institute; Dr. Carla Rodriguez-Watson, PhD, MPH, IMEDS Scientific Director, Reagan-Udall Foundation for the FDA; and Ramprasad Keshavamurthy, MBA, Sr. Director of Life Sciences Solutions, Saama Technologies for a live webinar on Tuesday, November 3, 2020 at 1pm EST.
For more information, or to register for this event, visit Active Surveillance: A New Paradigm in Patient Safety.
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