THE DIGITAL FOUNDATION FOR MODERN CLINICAL TRIALS

Meditrial’s integrated digital platform for the design, execution,
and oversight of global clinical trials.

Built to support medical devices, drug-device combinations, and pharmaceutical studies,Medigen Suite brings together data capture, imaging, trial operations, patient engagement, and compliance into one unified digital environment.

From first patient in to regulatory submission, Medigen Suite provides a continuous, connected, and compliant trial experience for sponsors, sites, and study teams worldwide.

A Unified Platform for End-to-End Trial Execution

Medigen Suite connects every aspect of a clinical study into a single operational ecosystem:

  • Clinical and imaging data

  • Site and study management

  • Patient-reported outcomes and remote participation

  • Regulatory compliance and audit readiness

All modules are fully integrated, allowing data, workflows, and oversight to flow seamlessly across the entire trial lifecycle.

Advanced Clinical and Imaging Data Capture

Catchtrial is Meditrial’s electronic data capture and image capture platform, designed for studies that require structured clinical data alongside imaging, device outputs, and specialized endpoints.

Everything You Need at Your Fingertips

Medigen Suite connects every aspect of a clinical study into a single operational ecosystem:

Catchtrial
EDC

Core electronic data capture for CRFs, study data management, monitoring, and reporting.

DICOM Imaging

Integrated medical imaging management for clinical trials with imaging endpoints.

Safety Adjudication

Conduct formal online safety adjudication using real-time dashboards that combine CRF data, source documents, and images.

ePRO/eCOA

Conduct formal online safety adjudication using real-time dashboards that combine CRF data, source documents, and images.

eConsent

Conduct formal online safety adjudication using real-time dashboards that combine CRF data, source documents, and images.

Site Payments

Conduct formal online safety adjudication using real-time dashboards that combine CRF data, source documents, and images.

Maptrial
CTMS

Maptrial is Meditrial’s clinical trial management system, providing a comprehensive view of trial operations across all sites and countries.

Maptrial
eTMF

Enable end-to-end tracking of regulatory documents across the study lifecycle, reducing startup delays and strengthening compliance.

Maptrial
eMVR

Maptrial eMVR gives sponsors and monitoring teams real-time, centralized visibility into clinical trial execution across all sites.

Trusted for Clinical Trial Compliance Globally

Powered by Meditrial’s Clinical & Regulatory Expertise

Medigen Suite reflects Meditrial’s decades of experience running complex global clinical trials.

The platform is continuously shaped by:

  • Medical and regulatory experts
  • Biostatistics and data science teams
  • Ongoing international studies

  • Interactions with regulators and notified bodies

This ensures the Suite evolves in alignment with real-world clinical and regulatory expectations.

A Platform That Scales
with Your Study

Whether supporting an early feasibility trial or a large, multinational pivotal program, Medigen Suite adapts to:

  • Study size and complexity

  • Site and country expansion

  • Hybrid and decentralized models

  • Evolving regulatory requirements

All within one unified, validated platform.

Upholding the Highest Compliance Standards

Medigen Suite is designed around global regulatory and quality standards, including:

Every data point, signature, workflow, and change is fully traceable and audit-ready, supporting confident regulatory submissions and inspections.