
Trial Planning & Management (CTMS)
Operational Planning. Study Control.
Maptrial® CTMS provides a centralized environment for planning, managing, and tracking clinical trial operations across studies, countries, and sites while maintaining full visibility and audit-ready oversight.
Teams can manage site activation, trial timelines, milestones, and operational activities from a single system. Built-in planning tools, progress tracking, and structured workflows help ensure studies stay aligned with protocol timelines and operational targets.

Online Monitoring (eMVR)
Centralized Monitoring. Complete Confidence.
Maptrial® eMVR enables sponsors and monitoring teams to oversee clinical trial execution across all sites from a single, centralized interface while maintaining compliance and full operational control.
Real-time visibility into data quality, visit progress, queries, SDV, freezes, and locks helps teams detect issues early and act quickly without disrupting site workflows.

Electronic TMF
Inspection-Ready Trial Documentation.
Maptrial® eTMF centralizes and manages essential clinical trial documents in a secure, structured environment, supporting regulatory compliance and consistent oversight across the study lifecycle.
Built-in document management, version control, and audit-ready processes help teams maintain complete and organized trial master files while staying aligned with regulatory expectations.

Site Payments
Financial Oversight. Simplified.
Maptrial® Site Payments provides sponsors and sites with centralized oversight of all clinical trial–related payments while maintaining transparency and financial control across studies and locations.
From a single interface, teams can track site-specific budgets, CRF- or visit-based payments, invoices, and credit notes. Automated calculations, bulk actions, and detailed reporting support efficient and compliant financial management throughout the study lifecycle.
Product Tracking
Supply Planning. Study Continuity.
Maptrial® Trial Supplies enables sponsors and study teams to forecast, manage, and track investigational product and ancillary materials across sites throughout the clinical trial lifecycle.
From planning supply needs to dispatching shipments, the system provides centralized visibility into inventory levels, site distribution, and supply status, helping ensure that study materials are available where and when they are needed.



