July 23, 2025
Accelerate Trials
Clinion CTMS is an integrated clinical trial management system that connects seamlessly with Clinion’s EDC, RTSM, and eTMF, and offers flexible integration with existing third-party systems. Its deep integration provides users with real-time visibility across the study, enabling timely interventions and adjustments that help accelerate study timelines.
Reduced Trial Costs
Customized workflows, pre-set processes, real-time status reports, automated alerts, and continuous monitoring provide holistic visibility, driving immediate and lasting efficiencies that significantly reduce trial costs.
Enhanced Visibility
Real-time Integration gives enhanced visibility into all aspects of the clinical research process - from study plan, design, site selection, subject recruitment, data capture, monitoring, remote monitoring, drug allotment, Inventory management and data management.
Feature-rich and Versatile
Gain complete trial oversight with a centralized CTMS system that unifies project tracking, monitoring, and financials. Manage key clinical research operations while delivering real-time visibility and operational clarity for CROs and sponsors.
Simplify Trial Operations and Collaboration with Clinion CTMS Software
- Project Management
Project ManagementEnables study project managers to manage studies remotely by setting up milestones and assigning CRAs (Clinical Research Associates) to studies and sites.
- IP Inventory ManagementIP Inventory Management
Efficient inventory tracking right from receipt to issue to returns. Product expiry and inventory replenishment notifications in real-time. Auto and manual indent management.
- Robust Financial
ManagementRobust Financial
ManagementOur dashboards and reports display milestones, payment receipts, expenses, dues and budgets that help monitor milestones and invoices alongside expenses entirely online.
- Advanced Dashboards
and ReportingAdvanced Dashboards
and ReportingImproved operational efficiency as our dashboards continuously monitor and display finances, projects, inventory and field results with effective reporting.
- Site MonitoringSite Monitoring
Enables Project Monitors and Clinical Research Associates (CRAs) to schedule monitoring visits across studies and CRAs to submit various monitoring reports approved by project managers.
- Document ManagementDocument Management
Manage all your study documents in one place so that they are accessible to both study and site personnel - Control who can access those documents and who cannot.
- Milestone & Task Tracking
Milestone & Task TrackingTrack trial milestones, assign responsibilities, and monitor task completion with automated reminders to ensure timely protocol adherence.
- Protocol Deviation Management
Protocol Deviation ManagementCapture, document, and track all deviations, corrective actions, and notifications to ensure compliance and trial integrity.
