Florence eConsent revolutionizes the way clinical trials manage consent documentation. Tailored for researchers and clinical trial managers, its intuitive interface enhances efficiency and reduces errors. Standout features include customizable workflows, electronic signature integration, and real-time audit trails.

What are the main features of Florence eConsent?

Customizable Workflows

Florence eConsent provides highly customizable workflows, allowing clinical trial teams to tailor processes to their specific needs. Designed for flexibility, this feature optimizes various stages of consent management:

• Streamline complex approval processes with adaptable templates.
• Integrate specific study requirements seamlessly.
• Automate notifications for faster follow-ups and approvals.

Electronic Signature Integration

The integration of electronic signatures simplifies participant consent, ensuring compliance while maintaining efficiency. This feature also helps reduce risks associated with paper-based consent:

• Facilitate remote consent processes with ease.
• Comply with regulatory standards effortlessly.
• Save time and reduce administrative burden.

Real-Time Audit Trails

Real-time audit trails in Florence eConsent offer transparency and accountability, essential for both trial sponsors and regulatory bodies. This feature enhances oversight and fosters trust in the trial process:

• Track document changes meticulously.
• Access a detailed history of user actions.
• Ensure data integrity and compliance with regular audits.