Florence Healthcare provides a Site Enablement Platform that automates document workflows and participant enrollment for clinical trials, enhancing collaboration among sponsors, CROs, and research sites. By connecting over 20,000 research sites globally, the platform streamlines clinical research processes, reducing operational risks and accelerating trial timelines.
Funding
$27M raised to dateRaised to date based on public sources. This may differ from the amount the company actually raised and is based only on what is publicly available on the internet.
Founders
Product
Problem
Clinical trials often suffer from inefficient document management, fragmented communication, and manual participant enrollment processes, leading to delays, increased operational costs, and potential compliance risks. Research sites and sponsors lack integrated platforms to streamline workflows and maintain real-time oversight across all study activities.
Solution
Florence Healthcare offers a Site Enablement Platform designed to digitize and automate clinical trial workflows, fostering enhanced collaboration between research sites, sponsors, and CROs. The platform provides solutions for document automation, remote monitoring, and participant enrollment, all within a unified environment. By digitizing document workflows and automating participant enrollment, Florence reduces operational risks, accelerates trial timelines, and improves communication among stakeholders. The platform's suite of products, including eBinders, eConsent, eNcounter, SiteLink, and eTMF, addresses key pain points in clinical research, ensuring compliance and streamlining study operations.
Target Audience
The primary users of Florence Healthcare's platform include clinical research sites, pharmaceutical sponsors, and contract research organizations (CROs) seeking to streamline clinical trial operations, enhance collaboration, and ensure regulatory compliance.
Features
- eBinders: Digitizes and automates investigator site files, participant binders, and logs, enabling remote monitoring for sponsors and CROs.
- eConsent: Facilitates secure and efficient digital workflows for informed consent, simplifying the consent process for both researchers and participants.
- eNcounter: Automates and centralizes participant enrollment, optimizing every stage of the participant journey with intelligent tracking tools and mobile-optimized assessments.
- SiteLink: Streamlines document distribution, monitoring, and exchange between sponsors and sites, regardless of their internal systems.
- eTMF: Provides an electronic trial master file with direct connectivity to study sites for seamless eISF document exchange.
- ParticipantLink: Enables sponsors to build and maintain a StudyReady database of potential participants, facilitating efficient matching with future studies.
- StudyOrganizer: Offers a free tool for research sites to manage study bookmarks, passwords, and contacts in one centralized location.
- Automated Compliance: Maintains compliant audit trails, controls access with role-based management, and streamlines electronic signatures.