Florence Healthcare


Florence Healthcare is a global leader in digital solutions for clinical trial sites, sponsors, and CROs. They aim to digitize every site, automate workflows, and accelerate studies through their site orchestration platform and research site solutions. Trusted by hundreds of sponsors, CROs, and over 37,000 sites across 90 countries, Florence Healthcare provides tools to streamline feasibility, study start-up, patient enrollment, remote monitoring, and compliance management. Their mission is to transform clinical trial operations by digitizing workflows and enabling efficient, compliant, and connected research environments.

Industries

biotechnology
health-care
pharmaceutical

Nr. of Employees

large (251-1000)

Florence Healthcare

Atlanta, Georgia, United States, North America


Products

Electronic investigator site file and binder management

Platform to digitize, automate, and integrate investigator site files, participant binders, and logs with remote monitoring capabilities.

Digital informed consent platform

Digital workflows for informed consent to support in-person and remote consenting, and to integrate consent records with study documentation.

Enrollment and screening automation platform

Centralizes and automates participant enrollment and screening workflows to optimize recruitment and eligibility processes.

Study information and credential manager

Repository for study bookmarks, passwords, and contacts intended for research site operational efficiency.

Document exchange and sponsor–site connectivity platform

Tools to distribute, monitor, and exchange study documents between sponsors/CROs and sites with audit logging and access controls.

Participant registry and candidate matching database

Database to maintain study-ready participant records and match candidates to appropriate studies, with routing to clinical sites.

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Services

Product demonstrations and onboarding

Scheduled product demos and onboarding sessions to evaluate platform fit and support initial deployment.

Compliance resources and guidance

Documentation and guidance on regulatory frameworks and compliance best practices for clinical trials.

Customer support and training / certifications

Customer support, training programs, and site enablement certifications to assist adoption and operational use.

Expertise Areas

  • Clinical trial site enablement
  • Digital health platforms for clinical research
  • Remote monitoring and source data access
  • eConsent and electronic consent workflows
  • Show More (3)

Key Technologies

  • Cloud-based clinical trial site enablement platform
  • Workflow automation
  • Digital informed consent (eConsent)
  • Electronic investigator site file (eISF) management
  • Show More (5)

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