Complion eConsent
The Leader in eRegulatory & Document Management for Clinical Trial Sites.
Overview
Complion is primarily an electronic regulatory binder system for clinical research sites. It includes an eConsent module that allows for the electronic signing and management of informed consent forms. The key advantage is the seamless integration of the consent process with the overall regulatory documentation workflow, ensuring that signed consents are automatically filed and managed in a compliant eISF.
✨ Key Features
- Integrated with eRegulatory/eISF
- 21 CFR Part 11 compliant signatures
- Remote and on-site consenting
- Automated document workflows
- Centralized document management
🎯 Key Differentiators
- Deep focus on regulatory workflows for sites
- High-touch customer support and implementation
- Purpose-built for site efficiency
Unique Value: Unifies eConsent and eRegulatory into a single, site-focused platform to reduce administrative burden and improve compliance.
🎯 Use Cases (3)
✅ Best For
- Streamlining regulatory and consent workflows at the site level
💡 Check With Vendor
Verify these considerations match your specific requirements:
- Sponsors or CROs looking for a standalone, multi-site eConsent solution
🏆 Alternatives
Provides a more specialized and comprehensive eRegulatory/eISF solution compared to broader platforms that may have eConsent as a less-developed feature.
💻 Platforms
🔌 Integrations
🛟 Support Options
- ✓ Email Support
- ✓ Phone Support
- ✓ Dedicated Support (Enterprise tier)
🔒 Compliance & Security
💰 Pricing
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