Streamline Regulatory Submissions

Unify operations for easier authoring and assembly

Veeva 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.

A real-time regulatory information feed, through our partnership with leading analytics provider Redica, turns data into actionable regulatory intelligence in the context of your portfolio.