Stop chasing insurance requirements and start advancing breakthroughs.
Lockton SAGE for Clinical Trials removes friction from managing global clinical trial insurance. By simplifying country-specific coverage placement, automating policy management, and centralizing critical documentation, it gives sponsors complete visibility and control across every trial jurisdiction.
One solution. One source of truth. Less time spent navigating insurance requirements and more time advancing research.
The result? Faster execution, greater confidence, and a clearer path back to breakthroughs.
Structured workflows reduce administrative work, so the information you need is available where and when you need it.
Country-specific intelligence and regulatory readiness give you real-time visibility across the full insurance lifecycle.
A centralized, auditable record of clinical trial insurance answers what was covered, when, where and why.
Specialists remain at the center, and technology extends their reach.

Global regulatory intelligence
Country-specific requirements, timelines and documentation guidance in one place. Export information from multiple countries into a single document.

Structures workflow management
Submissions, approvals, policy changes and status tracked through structured workflows with clear ownership.

Policy and document management
Policies, certificates and endorsements held with complete lifecycle visibility, plus expiration and renewal tracking.
Operational continuity
Version history, timestamps and documented rationale preserve institutional knowledge through team changes.
Connect with our life sciences specialists to learn how our Lockton SAGE for Clinical Trials can help you get back to breakthroughs.
Talk to our team