Implementing an eTMF is critical for Sponsors and CROs that want to reduce burden, increase study capacity, and enable more trials.
However, many organizations are not equipped with a modern solution to realize the full benefit and future proof operations.
With over 7,200 research sites connected to the Florence Network, we have an intimate understanding of the research site and the site’s eISF where over 80% of a TMF’s documents originate.
Through this uniquely qualified lens, we have compiled a complete guide to evaluating and implementing an eTMF that all stakeholders can appreciate. This guide covers:
- Impact of a Modern Active eTMF
- Benefits and ROI
- Compliance with FDA Regulations
- Selecting an eTMF Vendor
- Implementing an eTMF
- Site Collaboration
This guide serves as an in-depth overview of how a modern eTMF solution can impact your organization and the steps you can take to prepare.