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e-Regulatory Systems – Connecting Sites and Sponsors in a Whole New Way

Date: Aug 24, 2016 12:00 PM EST

As sites and sponsors continue to battle a growing regulatory burden, technology is shifting the clinical research industry towards electronic solutions that create efficiency while dramatically reducing costs. With innovative sites already implementing eRegulatory solutions around the world, it’s now easier than ever to eliminate paper-based regulatory binders at the site while streamlining regulatory processes from study startup to record archive. Learn how the newest eRegulatory system works and how sites and sponsors have successfully adopted this type of system to improve quality and efficiency.

This webinar explores:

· A global document management vision for the clinical research industry;
· Current regulatory challenges by research sites;
· Benefits experienced by sites, sponsors and CROs that adopt an eRegulatory system; and
· How sites can implement eRegulatory technology to standardize regulatory processes.


Nathan Levens

Product Manager, RealTime-CTMS Software Solutions

Nathan Levens, Product Manager for RealTime-eDOCS, has over 8 years of clinical research experience and spent over 4 years as the Quality Assurance Manager for one of the largest multi-specialty, phase 1-4 research sites in the US. Nathan has a deep understanding of research site processes and regulatory compliance challenges that shape our industry. He now teaches sites how to transition from paper-based regulatory processes to eRegulatory solutions such as RealTime-eDOCS to boost efficiency, drive compliance, and improve collaboration between sites and sponsors.


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