Free eBook | The Complete Guide to eRegulatory and eSource Blake Adams
Download The Ultimate Guide to eRegulatory and eSource for Clinical Trials
Everything you need to fully understand how eRegulatory and eSource will impact your clinical trial site – both the benefits and the challenges.
Benefits for Clinical Trial Sites
The Financial Impact
Avoiding Part-11 Compliance Mistakes
Selecting the Right Software Vendor
Best practices from over 2,000 leading Sites, Sponsors, and CROs
I feel more prepared to face the ever-changing landscape of research because of our relationship and partnership with Florence.
Clinical Trial Director, Academic Research Center
Research sites who fully implement an eRegulatory and eSource solution will see a 12.5% capacity increase, a 40% efficiency increase, and accelerate study startup by 25% – ultimately realizing $1.05M in ROI.
Ryan Jones, CEO, Florence
The most essential thing to do when moving to eRegulatory and eSource is developing a strong plan of action. Know what to look for in a vendor, the steps to implementing it at your site, and how you are going to accelerate user adoption.