WHY CLINICAL TRIAL SUPPLIES MATTER

Trials move at the speed of supply

Clinical trial supply is a critical path. When supply chain planning is late, fragmented, or inflexible, studies face delays, cost overruns, and there is disruption to patient continuity. Embedding quality, forecasting, governance, and execution directly into study delivery helps protect timelines, control costs, and keep patients on treatment across complex global trials.

WHAT IQVIA CLINICAL TRIAL SUPPLIES DELIVER

An end-to-end supply chain solution for study success

IQVIA delivers clinical trial supplies through an integrated, end-to-end solution that combines expert strategy, global sourcing, GMP packaging, compliant labelling, depot storage, temperature-controlled distribution, site and patient receipt, returns management, and certified destruction. Technology-enabled platforms ensure real-time visibility, regulatory compliance, and single-point of contact – optimising timelines, cost, and patient outcomes.
7,000+

Average drug shipments globally navigated by CTS annually

10+

Over a decade of clinical experience per Supply Chain Manager

15+

Supply Chain Manager presence in multiple countries globally

The IQVIA Clinical Supply team brought a steady, collaborative approach to what started as a lot of unknowns. They created the space to define both the “what” and the “how” together, shaping a new operating model. I especially appreciated the trust we built along the way and how fully they leaned into our mission. We’re excited about where this partnership can go next.
Emerging Biopharma
Clinical Supply Chain Lead

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