Ensure Seamless, Efficient Delivery Of Clinical Trial Materials Worldwide
By Carolyn Timpany, Senior Supplies Manager for the International Region, Lisa Spence, Director, Clinical Supply Chain for the International Region, and Ed Groleau, Director, Clinical Supply Chain for North America, PCI Pharma Services
With the number of registered clinical trials increasing significantly each year, it’s not surprising to learn that the clinical trials supply and logistics market is predicted to grow exponentially in the years ahead. This expected growth places huge pressure on drug discovery companies, CROs, and CDMOs to find supply management solutions which ensure seamless, efficient delivery of clinical trial materials worldwide, whilst navigating the challenges of more complex study designs and the ever-evolving regulatory landscape. PCI Pharma Services’ clinicalSMART™ is one such solution.
Designed with flexibility at its core, clinicalSMART™ is able to support sponsor requirements either throughout the entire study lifecycle, from protocol development through to final destruction of materials, or at time points when sponsor teams require additional resources to supplement in-house supply management expertise.
Review two case studies demonstrating how clinicalSMART™ operates.
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