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
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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.
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.
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.