VEEVA VAULT RIM
Regulatory Transformation
with Unified RIM
End-to-end regulatory information management on a single platform.
Vault RIM
The Vault RIM 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.
Stronger Compliance
Ensure teams are developing reliable regulatory content with high data integrity.
Global Alignment
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.
Vault Registrations

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 moreVault Submissions

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 moreVault Submissions Publishing

Veeva Vault Submissions Publishing incorporates publishing functionality within Vault RIM 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 moreVault 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 moreVault Connections

Vault Connections are Veeva-delivered integrations that seamlessly transfer data and documents between Vaults. For regulatory teams, the Vault RIM to Clinical Operations Connection enables users to automatically share product, study, and site information, the Vault Quality to RIM Connection shortens the overall timeline from change control event creation to implementation, and the Vault RIM to PromoMats Connection integrates compliance package generation for direct publishing to health authorities.
To see a full list of available Vault Connections, visit the Veeva Development Cloud page.
Vault RIM Essentials

Veeva Vault RIM Essentials is a cost-effective way for emerging biopharmas to get up and running on Vault Submissions and Submissions Archive in a matter of weeks. By leveraging customer best practices, Essentials provides an always up-to-date, multitenant cloud solution that equips small companies with a foundation for future growth.
Learn moreResources for Vault RIM



