The Florence Learning Library
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.
Read our extensive checklist on everything you need to consider regarding FDA 21 CFR Part-11 compliance for clinical trial electronic document management and workflows.
Learn about what the CCPA affects and the role both consumers and businesses play within this regulation.
You can enable remote site access for your clinical trial using these five steps.
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.
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.