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Florence eConsent

Connecting sites, sponsors, and CROs to advance research.

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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)

Academic medical centers Hospital research sites Commercial research sites Decentralized clinical trials (DCT)

✅ 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

Veeva SiteVault Complion Advarra

Unlike standalone eConsent tools, it's part of a comprehensive site platform, eliminating the need for integration between consent and regulatory binders.

💻 Platforms

Web API

🔌 Integrations

EHR/EMR systems CTMS 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 Florence eConsent Website →