CTMS
Coordinate study milestones, sites, monitoring activities, and study oversight.
The eTrialX platform
One platform.
Connected by design.
Clinical applications share a foundation that connects the people, processes, data, and documents behind every milestone. The platform can be tailored to your trial-specific workflows, processes, operational requirements, and governance.
The shared operational model
Modules share more than a menu.
Connect study context, people, process requirements, and evidence across clinical applications.
Clinical applications
The capabilities your teams work across.
EDC
Capture and review clinical data within the study’s shared context.
eTMF
Manage essential documents, versions, reviews, and supporting evidence.
LMS
Assign training, maintain completion records, and connect qualifications to readiness.
Site Portal
Connect site teams to assigned work, documents, and study communication.
Monitoring & RBM
Support monitoring activities, follow-up actions, and risk visibility.
Reporting & Analytics
Bring study performance, outstanding work, and readiness into view.
Governance & Audit
Apply access controls and retain traceable records of actions and approvals.
Intelligent processing
The connections do real work.
Rules evaluate conditions. Dependencies connect prerequisites. Workflows assign actions, route approvals, and escalate exceptions.
Integration capabilities are partially developed; external connections are assessed for each implementation.
Business rules
Define study-specific conditions and required checks.
Dependency-driven workflows
Initiate related tasks across clinical applications.
Exception management
Make blockers visible and route them to accountable owners.