Veeva Submissions | Regulatory content management | Veeva
Veeva Submissions
Streamline Regulatory Submissions
Submissions is a content management application used to plan, author, review, and approve regulatory documents. It provides full enterprise content management capabilities for creation, version control, approval, and real-time co-authoring for all submission-related documents. With content planning capabilities, users can build a submission outline and automatically match documents to the outline.
Clinical and non-clinical reports can be built and published using Report Level Content Plans. Dashboards and reports allow submission managers to track the status of each document in real-time.
Announced 2013 Status Very Mature Customers 100+
Download Product Sheet](/content/wp-content/uploads/2023/07/Veeva-Product-Sheet-Regulatory.pdf?1/index.html)
Discover how your regulatory team can become digitally mature
Veeva AI for Regulatory
Application Assistant Agent
Conversational insights into regulatory activities with clear and consistent narratives.
Impact
Exceed the likely outcome
15
of the top 20 companies use Veeva RIM
88
IT systems consolidated into one
90%
reduction in written standards
Why Veeva Submissions
Single authoritative source
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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.
Customer Success
Veeva RIM is trusted by 400+ top and emerging biopharmas
“The agile approach was instrumental in achieving that value in our end-to-end regulatory submission management processes.”
Paula Hudson, Senior Director of Global Regulatory Affairs
Eli Lilly
“For most system users, it will make their lives easier because they don’t have to upload duplicate documents or manage manual data entry”
Dee DeOliveira, Senior Director of Global Regulatory Operations
Cerevel
“We have this strong foundation to bring all of our data, content, processes, technology and have it fully integrated”
Vijay Reddi, Regulatory Transformational Lead
Roche
Resources
Explore and Learn
[Read Features Brief Veeva Submissions Features Brief
[Watch Demo End-to-End Veeva RIM Demo
[Read More Submissions Content Planning Feature Brief
[Watch Demo Submissions Content Planning Demo Video
[Read More Three Key Insights to Get the Most Out of Submission Content Plans
[View More Resources Veeva Connections Hub
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