Centralized Trial Oversight from Startup Through Closeout
Our CTMS solution provides a centralized platform for planning, managing, and tracking clinical trial operations across the study lifecycle. With real-time visibility into trial activities, milestones, and performance metrics, teams can reduce operational complexity, improve decision-making, and keep studies on track from startup through closeout.
Study planning and milestone tracking
Plan study timelines, define milestones, and track progress across sites and regions. Visual indicators help teams identify risks early and take action before timelines are impacted.
Real-time trial visibility
Monitor study health at a glance with dashboards that surface key operational metrics, risks, and status updates — enabling proactive decision-making throughout trial execution.
Visit and monitoring management
Manage site visits, monitoring activities, and follow-up actions in a structured, standardized workflow that improves consistency and accountability.
Centralized reporting
Keep monitoring visit reports and operational data in one place. Standard and configurable reports support ongoing oversight, internal reviews, and inspection readiness.
Streamlined collaboration across stakeholders
Enable efficient collaboration within the trial team with shared visibility into tasks, timelines, and study progress — reducing manual coordination.
Upholding the Highest Compliance Standards
Contact us for an introduction to Mednet's comprehensive EDC-centric eClinical platform with key native modules to support all study types and phases – such as randomization, trial supply management, adjudication, ePRO, payments, DICOM imaging, eConsent and more.