2026 Exclusive Insights

Wondering who will join you at Clinical Trial Supply Forum 2026? Download the attendee list for a preview of who you could meet on 12th-13th May in Amsterdam!

Are you truly cold-chain ready?

Cold-chain risk doesn’t announce itself with a major failure. More often, it creeps in through small gaps: an unqualified courier, a delayed customs clearance, a site without proper temperature monitoring, or packaging validated for best-case instead of worst-case conditions.

This practical, end-to-end checklist is designed to help you pressure-test your supply chain and uncover hidden vulnerabilities before they become costly problems.

With temperature-sensitive products now dominating modern clinical trials, cold-chain readiness has become one of the most important indicators of whether your trial stays on track – or faces delays, waste, compliance findings, and patient risk.

When you download this checklist, you’ll learn how to:

• Identify the seven highest-risk failure points across the cold-chain journey, from manufacturing release to direct-to-patient delivery
• Assess whether your organisation has the must-have controls, monitoring, and documentation that regulators expect
• Move from reactive firefighting to proactive, data-driven cold-chain risk management

If you are responsible for clinical trial supply, logistics, QA, or operations, this tool will help you evaluate where risk hides and what to do about it. Download the checklist now and benchmark your preparedness today.

Your clinical trial supply teams are being asked to do more than ever: move faster, manage greater complexity, protect temperature-sensitive products, stay compliant, and reduce waste, all while working with fragmented data and increasingly unpredictable trials.

If you’re responsible for ensuring investigational products reach patients safely, on time, and under the right conditions, understanding how to use data and AI effectively is no longer optional.

In this exclusive interview, Steve Jacobs, President, Global BioPharm Solutions, LLC, shares practical insight into how clinical trial supply leaders are already using AI, agentic systems, and data-driven decision-making to strengthen supply chain resilience, manage cold-chain risk, and support advanced therapies without compromising patient safety or regulatory compliance.

When you download this interview, you’ll learn how to:

• Build stronger data foundations that enable smarter forecasting, faster decision-making, and better supply continuity
• Use AI to reduce operational and cold-chain risk, particularly for advanced and temperature-sensitive therapies
• Adopt new technologies confidently while remaining inspection-ready, compliant with GMP, GDP, and GCP expectations

Download the interview now to gain expert-led insight you can apply immediately and equip your clinical trial supply operations for what comes next.