Veeva Vault Submissions

Streamline Regulatory

Unify operations for easier authoring and assembly.

Announced 2013
Customers 100+

Vault Submissions is the leading content management application used to plan, author, review, and approve regulatory documents. It provides full enterprise capabilities for creation, version control, approval, and real-time co-authoring of all submission-related documents.

With content planning capabilities, users can build a submission outline and automatically match documents to the outline. They can also build and publish clinical and non-clinical reports using Report Level Content Plans.

Dashboards and reports allow submission managers to track the status of each document in real time.

Vault Submissions manages the content creation workflow from planning through approval

Why Vault Submissions

Single authoritative source

  • Gain visibility

    Track progress through actionable reports and dashboards.
  • Accelerate time to market

    Automate multiple authoring and assembly tasks.
  • Align global teams

    Coordinate affiliate submissions and health authority interactions.

Exceed the
likely outcome


of the top 20 companies use Vault RIM


IT systems consolidated into one


reduction in written standards

Atara-Bio Bayer BeiGene Bluebird-Bio Brii-Biosciences Cerevel Dermavant GSK Jazz Krystal LEO
Luye Moderna MundiPharma Novo-Nordisk Regeneron Sarepta Servier UCB Vertex Zambon


Explore and learn

End-to-end Vault RIM demo
Watch demo
Guide to successful RIM implementation
Read best practices
Submissions Content Planning feature brief
Read more
Submissions Content Planning demo video
Watch video
Three Key Insights to Get the Most Out of Submission Content Plans
Read more
Vault Connections Hub
View more resources

Interested in learning more about how Veeva can help?