Successfully supplying clinical trials across the U.S., EU, and UK requires more than compliant manufacturing. International sponsors must also navigate complex import/export regulations, customs documentation, temperature-controlled logistics, and clinical supply management requirements. In Part II of this series, Experic CEO Matthew Mollan, Ph.D., explores the challenges of cross-border distribution, cold-chain integrity, inventory forecasting, and clinical trial resupply planning. Learn how proactive logistics strategies and an experienced CDMO partner can help sponsors minimize supply disruptions, reduce operational risk, and maintain the timely delivery of investigational products to clinical sites and patients.