A digital informed consent platform for clinical trials that enables remote and in-person participant consenting. It features real-time status tracking, electronic signatures, and audit trails to ensure regulatory compliance.
Florence eConsent is a specialized electronic informed consent solution designed to digitize and streamline the participant consent process for clinical trials. By replacing paper-based workflows with a secure, digital-first interface, it allows research sites to manage consent forms, track participant status in real-time, and maintain rigorous audit trails. The platform is built for flexibility, supporting both in-person and remote consenting, which helps sites accelerate study activation and improve participant comprehension. Key capabilities include a drag-and-drop consent builder, automated version control for protocol amendments, and secure remote access for monitors and regulatory bodies. As part of the broader Florence Trial Operations Platform, it integrates seamlessly with other site enablement tools like eBinders, providing a unified experience for research teams. While the platform is highly robust and compliant with global standards like 21 CFR Part 11, it is primarily targeted at clinical research sites and sponsors who require high-level security and inspection readiness.
Facilitates participant consent from any location, on-site or remotely, to accelerate study enrollment.
Provides visibility into participant progress through the consent process across study portfolios.
Supports compliant electronic signatures with integrated audit trails for regulatory verification.
Manages protocol amendments by distributing and tracking the latest consent versions automatically.
Enables secure remote identity verification for participants during the consent workflow.
Allows users to create and preview consent forms with a live editor.
Manages study staff permissions to ensure secure and compliant document handling.
Sends notifications to participants to improve completion rates and reduce study deviations.
Logs all regulated activities across the platform to support inspection readiness.
Supports Single Sign-On for streamlined access when used with the Florence eBinders platform.
Designed to meet international regulatory standards including FDA 21 CFR Part 11 and GDPR.
Provides controlled access for CRAs, IRBs, and regulatory agencies to review consent documentation.
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A digital informed consent platform for clinical trials that enables remote and in-person participant consenting. It features real-time status tracking, electronic signatures, and audit trails to ensure regulatory compliance.
Does Florence eConsent have an in-app market place?
Yes
How many Mini-Apps in the marketplace?
5
1. Florence eBinders - An add-on that allows users to create and manage digital binders for their clinical trial documents.
2. Florence eReg Binder - An add-on that enables users to consolidate and organize study regulatory documents in a digital format.
3. Florence eTMF Binder - An add-on that assists users in maintaining a complete and compliant eTMF for their clinical trials.
4. Florence eSource - An add-on that streamlines the process of capturing and managing source data electronically.
5. Florence eISF - An add-on that helps users maintain an inspection-ready Investigator Site File throughout the course of a clinical trial.
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Email Address
support@florencehc.comContact
(404) 937-1351Documentation
https://www.florencehc.com/support/documentation/Community Forums
https://community.florencehc.com/Chatbot
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