The Complete Guide To eRegulatory And eSource For Clinical Trial Sites

Transitioning to eRegulatory and eSource workflows is essential for clinical trial sites aiming to expand and advance their studies. Yet, numerous site leaders find themselves unprepared for this pivotal shift.

With more than 18,000 active clinical research sites on Florence eBinders, we have curated this comprehensive guide on eRegulatory and eSource. Its purpose is to aid trial sites in gaining a thorough understanding of:

• Benefits and ROI
• Compliance with FDA regulations
• Sponsor acceptance
• Selecting an eRegulatory and eSource vendor
• Implementing eRegulatory and eSource
• Ensuring user adoption

This guide is designed as an in-depth overview of how eRegulatory and eSource are impacting clinical trials, and the steps teams can take to prepare now.