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Catchtrial ePRO/eCOA/eConsent Apps

Patient-reported outcomes, electronic consent, and clinical outcome assessment for real-time, compliant data collection in clinical trials.

Solution by Meditrial
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Overview

Catchtrial ePRO/eCOA/eConsent Apps are a suite of electronic clinical data collection tools developed by Meditrial, designed to support patient engagement and data management in clinical trials. The suite is intended for use by patients, investigators, Clinical Research Coordinators (CRCs), and sponsors, and is built to meet GCP and FDA compliance requirements.

The Catchtrial platform consists of three integrated applications — ePRO (electronic Patient-Reported Outcomes), eConsent (electronic Informed Consent), and eCOA (electronic Clinical Outcome Assessment) — each addressing a distinct aspect of clinical trial data capture and participant management.

Catchtrial ePRO

  • Tracks complete patient data through a compliant, secure, and intuitive interface
  • Includes a user-friendly forms builder with easy data saving options
  • Fully integrated with eDiary for automated daily, weekly, and monthly patient data capture
  • Integrated with EDC (Electronic Data Capture) for real-time desktop access to patient-reported data
  • Facilitates interaction between the patient, investigator, and sponsor by analyzing patient health status data received directly from the patient

Catchtrial eConsent

  • Supports recruitment and informed consent management for clinical trials
  • Facilitates interaction between the patient and the Clinical Research Coordinator (CRC)
  • Uses telemedicine-inspired technology to allow researchers to obtain informed consent from participants remotely, from any location
  • Addresses common recruitment and consenting challenges through a proprietary Meditrial solution

Catchtrial eCOA — Key Features

  • Customized eCOA app that delivers step-by-step online guidance for the operator
  • Online training recording functionality for investigators
  • Automated score calculation, including Detection Threshold (DT)
  • Multilanguage functionality to support international trials
  • Complete audit trail ensuring GCP and FDA compliant data capture
  • One-click data exports through the central interface
  • Simple and intuitive interface designed to enhance the patient experience and improve data quality
  • Optimizes real-time data collection directly from patients

Meditrial operates across multiple international offices including New York, Berlin, Zurich, Rome, and London. The Catchtrial apps are positioned as integrated components within Meditrial's broader clinical data management offering, supporting streamlined and compliant data workflows across geographies.

Meta

Domain
Clinical Trial Management
Subdomain
Patient-Reported Outcomes (ePRO/eCOA) & Patient Engagement
Software type(s)
Workflow Automation
Deployment type(s)
Cloud / SaaS
Industry vertical(s)
BiotechCROMedical DevicesPharma
Development stage(s)
ClinicalPost-Market & RWE
Target user(s)
Research ScientistQA / Regulatory AffairsClinical / Diagnostic Professional
Compliance standard(s)
21 CFR Part 11GxP