Remove Paper from Your Document Approval Workflows with an eRegulatory Solution

Complying with regulatory requirements for cumbersome paper documents was challenging even before the pandemic hit. With the rise in hybrid and decentralized trials, the need for a eRegulatory solution is more important than ever before.

In this webinar, CCeReg Product Manager Alyssa Arce will explore:

• The current regulatory reality in clinical research
• The reasons why research organizations are making the switch
• How an eRegulatory solution can help remove paper from your document approval workflows.

This webinar will also include a free demo of CCeReg – our 21 CFR Part 11 compliant eRegulatory document management solution.

Download your copy!