Download the Complete Guide to eRegulatory and eSource for Clinical Research
This quick guide gives you everything you need to fully understand how eRegulatory and eSource will impact your clinical research, how to prepare for it, and how to ensure success.
- Benefits of eRegulatory for Clinical Trial Sites
- The Financial Impact and Return on Investment of eRegulatory
- Avoiding Part-11 Compliance Mistakes with eRegulatory
- Selecting the Right eRegulatory Vendor
- Ensuring User Adoption of eRegulatory
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Insights and Best practices from over 5,000 leading Clinical Research 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.