Modern eConsent Built For Clinical Research Sites

Clinical trial sites need to enroll patients faster while ensuring informed consent is compliant and well documented. Paper consent processes slow enrollment and create unnecessary administrative burden.

Florence eConsent digitizes informed consent so sites can collect, manage, and track patient consent electronically while maintaining regulatory compliance.mate document workflows, enable remote collaboration, and maintain always-on compliance.

Simplify Patient Consent with Florence eConsent

Digital Informed Consent

Replace paper consent forms with secure electronic workflows that allow patients to review and sign consent documents digitally.

Improve the Participant Experience

Interactive consent documents help patients better understand study procedures, risks, and expectations.

Simplify Consent Management

Track consent status, manage versions, and maintain complete documentation in one system.

Stay Inspection Ready

Electronic signatures, version control, and audit trails ensure consent records remain compliant.

Support Remote Consent

Enable patients to review and sign consent forms remotely or at the research site.

Get the Full eConsent Overview

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