Florence eConsent
Connecting sites, sponsors, and CROs to advance research.
Overview
Florence eConsent is part of the Florence eBinders platform, designed to streamline clinical trial processes. It allows research sites to consent participants electronically, whether they are on-site or remotely. The system is built to ensure compliance with regulations like 21 CFR Part 11 and HIPAA, and focuses on creating a seamless workflow from consent to filing in the eISF.
✨ Key Features
- 21 CFR Part 11 compliant eSignatures
- Remote and on-site consenting workflows
- Integration with eBinders (eISF)
- Version control for consent forms
- Audit trails
- Multimedia support for patient education
🎯 Key Differentiators
- Deep integration with its own eISF/eBinders platform
- Strong focus on site-level workflows
- Large network of existing research sites
Unique Value: A unified platform for sites to manage regulatory documentation and consent processes together, reducing administrative burden.
🎯 Use Cases (4)
✅ Best For
- Remote consenting for multi-site clinical trials
- On-site electronic consenting on tablets
💡 Check With Vendor
Verify these considerations match your specific requirements:
- Non-clinical research or simple surveys
🏆 Alternatives
Unlike standalone eConsent tools, it's part of a comprehensive site platform, eliminating the need for integration between consent and regulatory binders.
💻 Platforms
🔌 Integrations
🛟 Support Options
- ✓ Email Support
- ✓ Live Chat
- ✓ Phone Support
- ✓ Dedicated Support (Enterprise tier)
🔒 Compliance & Security
💰 Pricing
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