Use your VeevaID as a single login to all your Veeva products for sites. Learn more.
Manage study documents, monitoring, and patient consents across all your studies.
Manage digital patient consent forms, both on-site and remotely, through SiteVault.
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 exchange documents and read safety letters.
Work with your sponsor/CRO to manage patient randomization and trial supply.