Casestudy
Streamlining European expansion with integrated PV, regulatory, and commercial expertise
Learn how Cencora supported a US biopharmaceutical company preparing a multi-country EU/UK launch of an orphan medicinal product.
Key highlights
To simplify execution across markets, Cencora delivered a single-provider model combining pharmacovigilance with regulatory and commercialization support, including QPPV oversight, local PV system set-up, PSMF and SOPs, audits/CAPA, EV case management, literature monitoring, and aggregate reporting. The outcome was a scalable, audit-ready PV system that improved compliance and freed internal resources for growth.
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