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Medrio eConsent

eClinical solutions for every trial.

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Overview

Medrio eConsent is designed to simplify the informed consent process for participants, sites, and sponsors. It offers a flexible, intuitive interface for remote and on-site consenting. As part of the Medrio eClinical suite, it integrates seamlessly with their Electronic Data Capture (EDC) and ePRO solutions, providing a unified platform for patient data collection from the very beginning of a study.

✨ Key Features

  • Simple drag-and-drop form builder
  • Remote and on-site signing
  • Direct integration with Medrio EDC
  • 21 CFR Part 11 compliant
  • Real-time reporting on consent status

🎯 Key Differentiators

  • Speed and ease of study setup
  • User-friendly interface requires less training
  • Unified platform for EDC, eConsent, and ePRO

Unique Value: Delivers a fast, flexible, and easy-to-use platform for data capture and consent, enabling researchers to build and deploy studies in days, not months.

🎯 Use Cases (3)

Pharma, biotech, and medical device trials Diagnostics research Animal health studies

✅ Best For

  • Fast-paced clinical trials that require rapid study build and deployment

💡 Check With Vendor

Verify these considerations match your specific requirements:

  • Users who are not using or planning to use the Medrio EDC system

🏆 Alternatives

Castor EDC OpenClinica Veeva

Prioritizes speed and simplicity over the exhaustive feature sets of larger, more complex enterprise systems, making it a better fit for less complex or time-sensitive trials.

💻 Platforms

Web API

🔌 Integrations

Medrio EDC Medrio ePRO API

🛟 Support Options

  • ✓ Email Support
  • ✓ Live Chat
  • ✓ Phone Support
  • ✓ Dedicated Support (Enterprise tier)

🔒 Compliance & Security

✓ SOC 2 ✓ HIPAA ✓ BAA Available ✓ GDPR ✓ SSO ✓ 21 CFR Part 11

💰 Pricing

Contact for pricing
Visit Medrio eConsent Website →