Tracking and Adding Documents at Sites

During a clinical trial, CRAs (clinical research associates) collect and track numerous documents, including critical regulatory documents. CRAs can take advantage of the activity plans to generate a list of documents for tracking. In the document tracking views, they can also create their own lists of activities to track important dates.

Note: Regional study managers can use similar procedures to add and track documents at the region level in the Regions screen.

This task is a step in Process of Managing Sites and Contacts for Clinical Trials.