Clinical Supply Distribution Strategy – Planning & Adapting

A Clinical Supply Distribution Strategy must be solid enough to begin planning activities, and flexible enough to adapt to inevitable changes.

A good distribution plan starts with a clear idea of what countries the trial will be held in so that decisions can be made regarding the sourcing of the product, country label requirements, whether a depot is required, and QP considerations as needed.

In adapting a distribution plan to real-time changes, clinical supply managers must have mitigation strategies, a good foundation on how to adapt IRTs as necessary, and whether drugs can be returned for reuse.

In this article, our expert Neil Fox, PCI’s Clinical Supply Manager, covers how to ensure your Clinical Supply Distribution Strategy is robust and the information needed is available, how to best determine your depot requirements, how to efficiently adapt to study changes, as well as how COVID may impact your distribution planning.  Learn more by downloading the white paper below.

We provide a complete range of clinical supply services and we are committed to supporting clients at every stage of the clinical cycle, delivering best-in-class services efficiently and effectively.

Find out more about our Clinical Trial Services here


Our dedicated team of specialists will be happy to discuss any of your Clinical Trial needs. Contact us on +1 779-208-1819 (US) or +44 1495 711 222 (UK/EU) or email talkfuture@pciservices.com

When it comes to pharmaceutical and biopharmaceutical supply chain expertise who do you trust?

Your bridge between life-changing therapies and patients