Florence Login | Connect with Florence
The Florence Learning Library
A benchmark report of 143 global Clinical Research Associates (CRAs) who conduct remote monitoring through a digital link to the research site’s electronic Investigator Site File (eISF).
Explore how technology can make study start-up more efficient and compliant for sites.
Use this checklist to evaluate electronic consent solutions and determine what you need to ask vendors to reach your goals.
Learn about the latest trends in digital research technology from our 2021 mid-year report.
Check out this guide for an in-depth overview of how eRegulatory and eSource are impacting clinical trials and the steps you can take to prepare now.
Remote site access is now a requirement for clinical trial operations. Review this checklist to help you successfully assess solutions and modernize your approach to monitoring.
Over 400 pages answering 150+ questions sites have asked the FDA about using eRegulatory and eSource in clinical research.
We've gathered everything you need to know about choosing and implementing an eTMF into a single eBook. Download it before you choose an eTMF, or to get the most out of the eTMF you already have.
Wondering how GDPR affects the clinical trial industry? Check out the tips for complying with GDPR that we've gathered based on our experience working with European clinical research sites.
Wondering which eTMF software has all the features you need to run successful clinical trials? Use this checklist to evaluate eTMFs and choose the one that's right for your team.
Learn how sites and sponsors can plan their technology strategies today for the clinical
trials of tomorrow.
Use this checklist to avoid complications and headaches when implementing an eRegulatory solution by being equipped with the questions you should ask vendors.
600 Peachtree St. NE, Suite 920
Atlanta, GA 30308
Bulevar Kralja Aleksandra 84
11000 Belgrade, Serbia
© 2022. Florence Healthcare.