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.

Key capabilities include:

• eCRF and visit-based data capture
• Integrated image and waveform upload
• Validation and query management
• Adjudication and review workflows
• Secure, compliant data storage

Catchtrial supports both early feasibility and pivotal studies with the flexibility required for innovative trial designs.

Real-Time Study and Site Oversight

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

It supports:

• Site activation and readiness
• Enrollment and performance tracking
• Monitoring and quality oversight
• Milestones, payments, and vendor coordination
• Regulatory and inspection readiness

Maptrial enables study teams to manage complex trials with clarity, transparency, and control.

Built-In Digital and Decentralized Capabilities

Medigen Suite includes native tools to support modern patient engagement and decentralized trial models, including:

• ePRO and eDiary
• eConsent
• Remote and hybrid visit workflows
• Home-based data collection

These services are fully integrated into the same governed data and compliance environment as Catchtrial and Maptrial.

Medigen Suite is optimized for:

• Medical device and interventional studies
• Imaging-based endpoints and core lab workflows
• Combination products and hybrid trials
• Early feasibility through global pivotal programs

Its flexible architecture supports protocol-driven workflows, advanced data models, and multi-country regulatory requirements.

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

• ISO 14155
• ICH-GCP
• EU MDR and IVDR
• FDA 21 CFR Part 11
• Data integrity and traceability requirements

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

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.