Free eBook | The Complete Guide to eRegulatory and eSourceBlake Adams2018-06-01T11:26:06+00:00
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.