Expert insights for clinical trial logistics
Clinical trial shipments demand precise timing, uncompromising temperature control, and full chain-of-custody visibility—especially when managing investigational product, biological specimens, ancillary supplies, and multi-site distribution. This on-demand webinar breaks down everything teams need to know before moving trial materials across borders.
In this session, Mercury's specialists explain:
How to manage time- and temperature-critical investigational product (IP) shipments
Strategies for cold chain packaging and biological specimen handling
Best practices for direct-to-site and direct-to-patient distribution
How to navigate import licenses, IOR/EOR requirements, and customs complexities for clinical materials
Real examples: multi-site trials, comparator sourcing, ancillary supply kits, and depot-to-site distribution
Whether you manage clinical operations, regulatory affairs, or trial supply chain, this webinar gives you a practical playbook to reduce delays, protect product integrity, and manage risk.
What You'll Get
Full webinar recording
Actionable insights tailored for clinical trial logistics teams
Proven strategies used by leading pharma and CRO teams
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