Viedoc SDV Manager

Source data verification is one of the most time-consuming parts of clinical trial monitoring, and most teams are doing more of it than they need to. Viedoc SDV Manager gives study teams a structured, flexible way to take a risk-based approach to SDV, directly within Viedoc. 

In this webinar, we explore why a time-based approach to SDV more accurately reflects how risk actually occurs at a site, and demonstrate how Viedoc SDV Manager lets teams create, assign, and adjust SDV plans by date without requiring a CRF version change or study design update. 

Whether your team is still doing more SDV than necessary or already working toward a reduced approach, this session offers practical guidance on how to reduce verification effort where risk is low and increase focus where risk is elevated.

What you’ll learn

• How a time-based approach to SDV more accurately targets site risk than participant-based methods
• How to create, assign, and adjust SDV plans in Viedoc SDV Manager
• How targeted SDV supports risk-based monitoring and aligns with regulatory requirements
• Practical considerations for getting started, including how to enable SDV Manager in ongoing studies