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OpenClinica eConsent

Capture, manage, and analyze clinical research data.

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Overview

OpenClinica is a leading provider of open source clinical trial software. Their platform includes modules for EDC, ePRO, and eConsent. The eConsent feature allows for the creation of electronic consent forms that can be reviewed and signed by participants on a tablet or computer, ensuring a compliant and auditable process that feeds directly into the main clinical database.

✨ Key Features

  • Open source option available
  • Integration with OpenClinica EDC
  • 21 CFR Part 11 compliant eSignatures
  • Role-based access control
  • Audit trails

🎯 Key Differentiators

  • Availability of a free, open-source community edition
  • Strong focus on data standards (CDISC)
  • Flexible and extensible platform

Unique Value: Provides a flexible, standards-compliant, and open-source-based platform for clinical data management and eConsent, offering control and cost-effectiveness.

🎯 Use Cases (3)

Academic research Biotech and medical device companies Global health research

✅ Best For

  • Clinical trials requiring a flexible and cost-effective EDC/eConsent solution

💡 Check With Vendor

Verify these considerations match your specific requirements:

  • Organizations without any technical resources (for the open-source version)

🏆 Alternatives

REDCap Castor EDC Medidata

More powerful and compliant for clinical trials than REDCap, but more accessible and flexible than large, closed-off enterprise systems.

💻 Platforms

Web API

🔌 Integrations

API

🛟 Support Options

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

🔒 Compliance & Security

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

💰 Pricing

Contact for pricing

✓ 30-day free trial

Visit OpenClinica eConsent Website →