Veeva Help for Sites

Help articles, release notes, and product information for clinical research sites

Use your VeevaID as a single login to all your Veeva products for sites. Learn more.

26R3 Release - December 2026 Check out the features introduced in 26R3! See What's New

Manage study documents, monitoring, and patient consents across all your studies.

Work with your sponsor/CRO to exchange documents and read safety letters.

Work with your sponsor/CRO to collect and manage patient data.

Work with your sponsor/CRO to collect and manage clinical outcome assessments.

Work with your sponsor/CRO to complete training for a specific study.

Work with your sponsor/CRO to manage patient randomization and trial supply.