By Christopher Engel
Across Europe, network design studies—often called “distribution studies”—are no longer rare. They have become a standard step for pharmaceutical and healthcare companies seeking to optimize their supply chains. Post-pandemic resilience, cost pressures, and ambitious sustainability targets are driving this shift toward network optimization, often resulting in fewer distribution centers and a reduced number of logistics service providers.
These studies frequently evolve into RFIs, RFPs, or RFQs. The decisions made during the design phase can significantly impact cost, compliance, and service quality. That’s why involving logistics partners early is critical.
Network design is not just about theoretical efficiency. It must account for regulatory compliance, operational feasibility, and service continuity. Choices such as where GMP labelling occurs, how QA release is sequenced, and how cross-border flows are managed can turn an “optimal” design into a costly or noncompliant reality.
By engaging 3PL providers from the start, pharma companies can:
In Central Eastern Europe, a proposed leaner network looked ideal on paper: fewer sites, lower unit costs. However, once real-world factors were applied—extra kilometers, double handling, GMP labelling—the TCO exceeded expectations. The RFQ that followed was unsuccessful, with market pricing landing 25–30% above the client’s benchmark, particularly in warehousing and labelling. Timing for site readiness also conflicted with the desired go-live date.
Early involvement of logistics partners could have prevented these misalignments.
Key Principle: Early collaboration with 3PL providers ensures pragmatic, compliant, and cost-effective network designs—turning studies into successful RFIs, RFPs, and RFQs.
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