Maptrial no icon logo

Centralized governance for global trials.

Maptrial no icon logo

Centralized governance for global trials.

Medigen® CTMS+ centralizes planning, monitoring, document management, product oversight, and finances to streamline trials, reduce costs, and deliver faster, smarter results.

Maptrial
Maptrial

Streamline clinical trial operations with centralized efficiency and real-time insights.

Trial Planning & Management (CTMS)

Trial Planning & Management (CTMS)

Monitor your clinical trials remotely and automate issue detection for global success.

Online Monitoring

Online Monitoring (eMVR)

Track site performance remotely and ensure data accuracy in real time.

Electronic TMF

Electronic
TMF

Track regulatory documents throughout the study lifecycle, ensuring timely completion of all required materials.

Site Payments

Site
Payments

Simplify site payments, automate invoice generation, and track disbursements across all sites, with alerts to prevent delays.

Product Tracking

Product
Tracking

Manage trial supplies efficiently, track shipments, and forecast inventory at each site to maintain study timelines.

Trial Planning & Management (CTMS)

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.

  • Study, country, and site planning with activation tracking
  • Milestones, timelines, and operational activity management
  • Operational dashboards for enrollment, progress, and site performance
Online Monitoring

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.

  • Real-time oversight across sites and study activities
  • Visual risk indicators and automated monitoring checks
  • Role-based controls with complete audit trails
Electronic TMF

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.

  • Centralized document management and version control
  • Audit-ready framework supporting regulatory compliance
  • Integration with EDC, CTMS, and operational workflows
Site Payments

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.

  • Centralized tracking of site payments and budgets
  • Automated calculations linked to visits or CRFs
  • Invoices, credit notes, and detailed financial reporting
Product Tracking

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.

  • Forecasting of investigational product and ancillary supplies
  • Shipment planning and site distribution tracking
  • Centralized visibility of inventory and supply status