Turn clinical trial complexity into structured execution.

Fewer bottlenecks. Faster decisions. Built-in control.

Judi is the only platform built to manage and orchestrate all of your clinical trial processes. It optimizes your teams’ performance with structured, integrative, collaborative workflows to prevent breakdowns at handoffs between stakeholders and systems.

A single unified workspace, applied across critical trial workflows

Used by sponsors, CROs and AROs to manage high-stakes processes across clinical operations, medical affairs, and safety including:

  • Eligibility: Centralized, structured eligibility review to enhance protocol compliance and improve oversight.
  • Site qualification: Documented assessments of site readiness, capabilities and compliance before activation to support site performance.  
  • User qualification: In-platform training and qualification, so the right users have the right access and know-how before using the platform.
  • Endpoint adjudication: Structured, auditable endpoint case processing and review workflows to support consistent decisions and defensible outcomes.
  • DSMB: Streamlined committee workflows for data review cycles, meetings, follow-up actions and recommendations.  
  • Imaging: Compliant imaging collection, transfer, storage and analysis with full traceability.
  • Remote SDV: Secure remote source document verification and follow-up for efficient data cleaning.
  • Platform flexibility: Configurable steps, roles and approvals to fit your study requirements across any workflow.

From our clients

“Your exceptional response time and solution-oriented approach have consistently exceeded our expectations, empowering our teams to achieve remarkable results.”

– Executive Director, Safety Medical Sciences, Top Three CRO

"Judi is critical to making trials happen—connecting all the pieces. It has the power to enable us, protect information and exchange data."

– Leading Imaging Core Lab

"Information flow wouldn't happen [without Judi]... it's the conduit/glue for information transfer among stakeholders.”

– Leading Medical Device Sponsor

                Trusted by 5 of the top 6 global CROs, plus