Vault RIM Suite
The Vault RIM Suite streamlines global regulatory processes on a single, cloud-based platform, enabling life sciences companies to improve visibility, data quality, and agility.
Speed to Market
Respond faster to changing regulations and increase process efficiency from submission planning to publishing.
Ensure teams are developing reliable regulatory content with high data integrity.
Coordinate regulatory efforts across HQ, affiliates, and partners within a single RIM system.
Unified and Connected
Tackle cross-functional business processes as part of the Veeva Development Cloud.
Veeva Vault Registrations manages product registration data worldwide, including registration status, variations, and health authority interactions. Veeva’s flexible data model accommodates IDMP data points and will continue to support evolving regulatory data standards. Watch this short video on Veeva's approach to IDMP.Learn more
Veeva Vault Submissions streamlines submission planning through approval by automating regulatory process steps. Users can create submission content plans, render submission-ready documents, and track submission status with complete traceability.Learn more
Vault Submissions Publishing
Veeva Vault Submissions Publishing incorporates publishing functionality within the Vault RIM Suite for end-to-end submission development. By employing a continuous publishing process to create, validate, and submit dossiers, users can dramatically speed submission delivery.Learn more
Vault Submissions Archive
Veeva Vault Submissions Archive stores a complete history of regulatory submissions securely in the cloud. Affiliates can download submissions or submission components for reuse in local markets and upload their submissions to local health authorities.Learn more
To see a full list of available Vault Connections, visit the Veeva Development Cloud page.