Case study

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.
European expansion white paper thumbnail

Download to learn more

Pardot Form

We’re here to help

Connect with our team today to learn more about how Cencora is helping to shape the future of healthcare.
abstract

Related resources

Article

Harmonizing and safeguarding global and local pharmacovigilance processes

Webinar

Applying AI and analytics to improve lifecycle benefit-risk assessment
Discover the significance of ISO 9000 certification for manufacturers

White paper

Competing through complexity: Models to manage mature products