Clinion CTMS

Clinion CTMS is a clinical trial management system designed to help sponsors and CROs plan, track, and manage clinical trial operations across Phase I–IV studies. The platform centralizes study oversight, site management, milestone tracking, protocol deviation management, financial operations, and reporting within a single system. Through integration with EDC, RTSM, eTMF, and third-party applications, Clinion CTMS provides a unified view of clinical, operational, and regulatory activities, helping teams improve coordination and execution across the trial lifecycle.

Key Capabilities

Protocol Deviation Management

Captures, documents, and tracks protocol deviations through a centralized repository. Automated notifications and standardized workflows support timely review and resolution while maintaining study oversight.

Study Milestone Tracking

Provides end-to-end visibility into study progress from initiation through database lock. Real-time milestone monitoring and deviation tracking help teams manage timelines and identify potential delays.

Reports and Letters Management

Supports the creation, review, approval, and tracking of study reports and correspondence. Automated workflows help ensure consistency, accountability, and compliance across sites and study teams.

Financial Management

Centralizes invoice management, expense tracking, site payments, and financial reporting. Milestone-based invoicing and audit-ready financial records provide greater visibility into study finances.

System Administration and Configuration

Allows organizations to configure approval hierarchies, workflows, notifications, financial rules, and operational settings to align with internal processes and governance requirements.

Integrated Trial Oversight

Connects with EDC, RTSM, and eTMF systems to provide unified access to clinical, operational, and regulatory data. Flexible integration capabilities support connectivity with third-party applications.

Key Benefits