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Pharmacovigilance deals with the collection and analysis of post-approval data for drugs to ensure they are safe for long-term use. As therapeutics continue to become more complex and tailored to each patient, biopharma companies will face new challenges in tracking adverse reactions and complying with pharmacovigilance guidelines established by diverse regulatory agencies around the world. Pharmacovigilance webinar topics include strategies for outsourcing and managing safety reporting in emerging markets.