CTMS is a centralised Clinical Trial Management System designed to plan, track, and control every operational aspect of late-phase clinical trials. By integrating study planning, site management, monitoring, and financial oversight into a single platform, CTMS delivers real-time visibility, improves coordination across sponsors, CROs, and sites, and supports compliant, efficient execution across global studies.
Delivers centralised visibility into all clinical trial operations for informed decision-making.
Improves coordination between sponsors, CROs, and sites through shared, real-time information.
Accelerates study start-up and site activation timelines through structured workflows.
Provides better control over timelines, budgets, and resources across complex trials.
Reduces operational risk and compliance gaps with proactive issue and risk management.
Ensures trial management activities are continuously audit-ready and inspection-ready.
faster study start-up timelines
improvement in site performance visibility
reduction in operational delays and rework
auditable clinical trial management activities
