Florence eTMF is a robust software designed to optimize clinical trial management by digitizing and organizing essential trial documents. Targeted towards research teams and healthcare organizations, this solution enhances collaboration, speeds up processing, and ensures compliance with its innovative electronic Trial Master File system.

What are the main features of Florence eTMF?

Enhance Collaboration Across Teams

Florence eTMF facilitates seamless interaction among research teams, providing a centralized platform for document sharing and communication. By integrating key collaboration tools, it ensures that team members remain connected and synchronized, no matter where they are located.

• Centralized document repository
• Real-time collaboration capabilities
• Access control for team roles

Accelerate Document Processing

Designed to speed up the document handling process, Florence eTMF automates many of the tedious tasks associated with traditional document management in clinical trials. This results in significant time savings by minimizing manual entry and reducing errors.

• Automated document indexing
• Efficient workflows to manage approvals
• Version control and audit trails

Ensure Regulatory Compliance

Your compliance requirements are at the forefront of Florence eTMF's capabilities. The software delivers comprehensive documentation solutions that adhere to global standards, ensuring research operations are always regulation-ready.

• Supports 21 CFR Part 11 compliance
• Real-time monitoring of regulatory changes
• Comprehensive compliance reporting