Medable eCOA+ is a cloud-based platform for electronic Clinical Outcome Assessments (eCOA) and electronic Patient-Reported Outcomes (ePRO), designed to streamline and automate data collection in clinical trials. The platform integrates with eConsent, telehealth, and digital sensors, supporting a unified workflow for sponsors, sites, and participants. With a library of over 380 pre-validated instruments, AI-powered automation, and support for BYOD and provisioned devices, Medable eCOA+ accelerates study deployment, enhances data quality, and improves patient engagement across diverse therapeutic areas and geographies. The system is globally compliant and offers real-time analytics, notifications, and 24/7 support for seamless trial operations.

Key Features

Pre-Validated Instrument Library Access to 380+ reusable, scientifically reviewed and validated eCOA/ePRO instruments.

• Standardizes data collection across studies
• Reduces study build and validation time

AI-Enabled Automation Automates repetitive and manual study setup tasks.

• Reduces study build timelines by up to 50%
• Accelerates time to First Patient In (FPI)

Unified Platform Integration Combines eCOA, ePRO, eConsent, telehealth, and sensor data in one system.

• Seamless workflow for sites, sponsors, and participants
• Supports digital physiological measures from wearables and sensors

BYOD and Provisioned Devices Supports both participant-owned and provisioned devices.

• Increases accessibility and patient reach
• Enables participation across geographies and demographics

Real-Time Data Capture and Analytics Captures objective and subjective data in real time.

• Enables immediate insights and decision-making
• Submission-ready data for regulatory compliance

Global Compliance and Localization Available in 70+ countries and 120+ locales.

• Adheres to FDA, CFR21 Part 11, HIPAA, and GDPR standards
• Multilingual support for global trials

24/7 Global Support Round-the-clock support for sites, patients, and study teams.

• Ensures high user satisfaction and protocol compliance
• Facilitates seamless technology adoption

Benefits

Accelerated Study Start-Up Significantly reduces time to deploy and launch clinical trials.

• AI and automation cut study build time by up to 50%
• Enables rapid response to evolving research needs

Improved Data Quality and Compliance Standardized, validated instruments and automated workflows reduce errors.

• Ensures regulatory compliance and audit readiness
• Enhances reliability of clinical trial outcomes

Enhanced Patient Engagement and Retention Consumer-grade UX and flexible device options improve participation.

• Reduces patient burden and increases retention
• Supports inclusivity across diverse populations

Operational Efficiency Unified platform and automated processes streamline trial management.

• Reduces manual entry and administrative workload
• Facilitates real-time monitoring and reporting