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+
Discover how your regulatory team can become digitally mature
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.
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
Customer Success
Veeva RIM is trusted by 400+ top
and emerging biopharmas
Resources
Explore and Learn
Watch demo
End-to-end Veeva RIM demo
Read best practices
Guide to successful RIM implementation
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Submissions Content Planning feature brief
Watch video
Submissions Content Planning demo video
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Three Key Insights to Get the Most Out of Submission Content Plans
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