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ePro Overview:

Platform Type: Web-based SaaS
Primary Use: Patient-Reported Outcomes & Data Collection

ePro is an electronic patient reported outcome (ePro) system designed by Landmark Research, which is offered as a software as a service (SaaS) for its clients to collect data via ePro devices to enable the clients to manage the subject's questionnaires and diaries in their clinical studies.

ePro is a web-based platform that allows the users to perform the following functions:

EDC System Features

Secure • Reliable •
Compliant

Core Functions

ePro provides comprehensive patient-reported outcome data collection and management capabilities for clinical trials with advanced analytics and compliance features.

  • ePro Data Collection

  • ePro Data Management

  • Data Analysis & Reporting

  • Regulatory Compliance

  • ePro Data
    Collection

    ePro enables users to collect data from subjects using various devices including smartphones, tablets, computers, and wearable devices. It supports various data types such as symptoms, quality of life, satisfaction, adherence, and preferences, with multiple collection modes.

  • ePro Data Management

    ePro enables users to manage collected data using tools for validation, cleaning, encryption, backup, and export. It ensures data quality, integrity, and security while maintaining compliance with FDA, EMA, and ISPOR guidelines and regulations.

  • Data Analysis & Reporting

    ePro enables users to analyze and report data using descriptive statistics, inferential statistics, psychometric analysis, and PRO measures. It offers data integration, visualization, and analytics services while ensuring compliance with CONSORT, ISOQOL, and PROQOLID standards.

Talk to our ePro experts

Speak with our ePro specialists to learn more about our electronic patient reported outcome system, request a demo, or get help with implementation. Our dedicated team is ready to assist you with all your clinical trial patient-reported outcome data collection and management needs.

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