The Florence Learning Library
Over 400 pages answering 150+ questions sites have asked the FDA about using eRegulatory and eSource in clinical research.
Learn about what the CCPA affects and the role both consumers and businesses play within this regulation.
Learn how sites and sponsors can plan their technology strategies today for the clinical
trials of tomorrow.
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.
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.
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.
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.
Make implementing your new eRegulatory software seamless. This eBook shares how to choose the right vendor, build an implementation team, and encourage adoption of new technology among your users.
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Download this eBook of cloud computing and clinical research terms to help your team quickly and accurately evaluate eClinicial platforms.
Explore this interactive guide on how to successfully evaluate, select, and implement eRegulatory software at your organization.
Read this guide to avoid being locked into a single clinical trial software vendor and to ensure your technology systems can integrate with one another.
Learn tips for conducting clinical trial monitoring visits throughout the life of a study and gain insights into how technology is transforming the monitoring visit.