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Tuesday
, March 28 • 11:45am - 12:30pm
BENEFIT-RISK ASSESSEMENT FOR DRUG AND BIOLOGICAL PRODUCTS
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What, Why and How is BRA done across the Product Life Cycle
Analyze FDA's B-R framework
How can limitations/uncertainties be tackled/addressed
Discuss different initiatives and the future
Speakers
Siva Kumar
Global Phv Surveillance Physician Sr Manager, TEVA
Tuesday March 28, 2023 11:45am - 12:30pm EDT
Le Méridien Philadelphia
General Session