Protocol amendments without the meltdown: Handling mid-study changes in Viedoc

Mid-study changes are inevitable in clinical trials. Protocol amendments, design tweaks, new forms, SDV adjustments – we all know they're coming. The question isn't if, it's how to handle them without losing hours or compromising data integrity.

In this session, we'll walk through real-world scenarios that data managers face daily: simple edits to edit checks, adding new forms with repeating item groups, handling changes that affect SDV validation, and managing the documentation that comes with it all. We'll show you how Viedoc's design version management capabilities let you make these changes quickly and confidently, while keeping a complete audit trail throughout the system.

We'll move through our product suite to show you exactly how these tools work together to streamline the amendment process. By the end, you'll see how what might have taken hours can be handled in minutes – without the stress.

If you've ever wondered how to keep mid-study changes from derailing your timeline, this is the session for you.