Patient-centered data for smarter, faster trials.

Catchtrial® Apps+ foster patient engagement, increase retention, and deliver high-quality patient outcome data, enabling smarter, faster, and more efficient trials.

Digital-first electronic
outcomes for any trial.

Catchtrial® Apps+ replace paper documents and fragmented tools with a secure, intuitive digital experience. Patients and clinicians capture outcomes from anywhere, on any device — reducing site burden while improving data quality and protocol adherence.

Catchtrial® ePRO

Capture and manage Patient-Reported Outcomes on a centralized platform.

Catchtrial® ePRO is a digital patient-reported outcomes solution enabling direct delivery and return of health status surveys to capture symptoms, diaries, and quality-of-life data in real time.

Catchtrial® eCOA

Optimize data collection directly from patients in a streamlined way.

Catchtrial® eCOA is a digital clinical outcome assessment solution enabling real-time patient-reported data capture through an intuitive interface to enhance patient experience and improve data quality.

Catchtrial® eConsent

Facilitate better interaction between the patient and the Clinical Research

Catchtrial® eConsent is a digital informed consent solution leveraging telemedicine technology to streamline recruitment, enable remote participation, and enhance patient engagement and data quality.

Say goodbye to paper surveys.

Build for Privacy & Complaince

Catchtrial® enables secure patient onboarding and end-to-end data oversight through a privacy-first architecture designed to meet global regulatory and inspection-readiness requirements.

  • No collection of participants’ sensitive data (GDPR and HIPAA compliant)

  • Complete patient data tracking system (ICH/GCP and 21 CFR Part 11 compliant)

  • Easy and secure patient registration via Catchtrial QR code

Say goodbye to paper surveys.

Intuitive ePRO Survey Management

Catchtrial® ePRO offers an intuitive, no-code survey design experience with seamless participant engagement and reliable data continuity throughout the reporting process.

  • User-friendly ePRO Forms Builder interface (no programming skills required)
  • Intuitive and engaging user interface
  • Send/Resend survey invitations

  • Easily save and persist data

Say goodbye to paper surveys.

Unified Patient-Reported Data Flow

Catchtrial® ePRO delivers a patient-friendly reporting experience with automated diary-based data capture and seamless EDC integration for real-time access to patient-reported outcomes.

  • ePRO patient survey forms are easy and simple for patients to fill out

  • Integrated eDiary for routine automated patient data capture (e.g. daily, weekly, monthly)

  • Full integration with EDC for real-time desktop access of patient-reported data

Redefining How

Trials Are Run

Collect data in a streamlined, compliant
and efficient way.

Catchtrial® eCOA is a flexible digital outcome assessment platform supporting intuitive data capture and global instrument deployment, enhancing patient engagement and study execution.

  • End-to-End eCOA Ecosystem

  • Modular and Flexible Configuration

  • Multi-Stakeholder Outcome Data Capture

  • Customized eCOA Application with Guided Workflows

  • Centralized Data Access and Export

  • Integrated Investigator Training Resources

  • Automated Scoring and Calculations

  • Global Multilanguage Support

  • Comprehensive Audit Trail

Train and Enable Investigators

Investigators are supported through a customized eCOA app that delivers step-by-step, online guidance for standardized assessments, complemented by on-demand training recordings to ensure consistency across sites.

Standardize Assessments & Scoring

Automated score calculations—such as Detection Threshold (DT)—are performed within the eCOA app, reducing variability, eliminating manual errors, and ensuring consistent data capture across all operators.

Ensure Compliance & Data Readiness

A complete audit trail supports GCP and FDA-compliant data capture, with one-click data exports available through a centralized interface for rapid review, monitoring, and analysis.

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.

Accelerate your clinical trials worldwide.

Our decentralized, trial apps streamline data capture & management — delivering faster, more efficient results.

Expand outreach, boost trial enrollment.

Overcome recruitment and consenting challenges by customizing outreach to a broader range of participants, boosting enrollment rates effectively.