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.

Introducing

Maptrial streamlines clinical trials with a centralized platform for planning, monitoring, & finances, boosting efficiency and cost savings.

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

Trial Planning & Management (CTMS)

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

Electronic
TMF

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

Online Monitoring
(eMVR)

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

Site
Payments

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

Contracts
Payments

Simplify trial payments, generate invoices, and analyze costs at both study and site levels, with alerts to prevent delays.

Trial
Supplies

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

Site Document Tracker

Centralize site documents, monitor regulatory submissions, track updates in real time to reduce administrative burden.

Trial Planning & Management (CTMS)

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

Accelerating Trial Recruitment & Outcomes

Accelerating Trial Recruitment & Outcomes

Overcome recruitment and consenting challenges by Meditrial proprietary telemedicine-inspired product called Catchtrial® eConsent. eConsent allows researchers to obtain informed consent from participants from anywhere using telemedicine technology.

Catchtrial eConsent enables participants to review and sign informed consent from anywhere using telemedicine-inspired technology. Compatible with Android and iOS, it removes the need for on-site visits and provides a seamless, mobile-first experience for patients.

The app guides participants step by step, presenting study information clearly and assessing comprehension. This patient-centric approach improves engagement, ensures understanding, and enhances data quality across your trial.

Supporting decentralized trial workflows, Catchtrial eConsent significantly reduces the time required for screening and enrollment. Faster, smoother consent processes allow trials to progress efficiently while keeping patients and sites aligned.

Consent from participants or their legally authorized representatives (LARs) is securely captured and stored. The platform maintains a complete audit trail, enabling regulatory compliance and real-time tracking to keep your trial on schedule.

Handle complexity.
Set everything straight.

Track regulatory documents through the study life cycle to ensure timely completion, reduce delays, and improve compliance.

Maximum trial quality and instant validation.

Catchtrial enhances clinical trial monitoring by identifying missing data, flagging violations, automating follow-ups, & sending notifications for better quality control.

Real time analysis for better decisions sooner.

Catchtrial provides instant data access, enabling custom visualizations and progress tracking for your study.