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Challenges in Generic Drug Safety and Surveillance - FDA Generic Drugs Forum 2018 (Kazi Aayan) View |
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What Students Need To Know About Post Marketing Pharmacovigilance Practice at FDA (British BioMedicine Institute) View |
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GDUFA II (9/28) Generic Drugs Forum 2017 (U.S. Food and Drug Administration) View |
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FAERS (April 2015) (U.S. Food and Drug Administration) View |
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FDA’s Role in Foreign Drug Manufacturing (November 2017) (U.S. Food and Drug Administration) View |
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Regulatory Framework for Medicinal Product Distribution in the United States: An Overview (Dr.Pooyan Ghamari, PhD) View |
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Introduction to Post-Approval/Generics track with Ryan Franke (Simulations Plus, Inc.) View |
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Understanding the FDA Approval Process for Gene Therapies: Step-by-Step Explanation (ShareTreck) View |
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ANDA Policy and Regulatory Considerations Prior to Filing (12/28) Generic Drugs Forum 2017 (U.S. Food and Drug Administration) View |
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Dr. Richard Hansen - Advancing the Science of Drug Safety (Auburn University) View |