## 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**](/content/resources/journey-to-digital-maturity-for-regulatory/index.html)

##### Veeva AI for Regulatory

###### Application Assistant Agent

Conversational insights into regulatory activities with clear and consistent narratives.

**[See it in action](/content/resources/application-assistant-agent/index.html)**

###### 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

Press O for more options

Click for sound

#### 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

[Read case study](/content/customer-stories/eli-lilly-accelerates-rim-deployment-with-agile-approach/index.html)

“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

[Watch video](/content/customer-stories/improving-cross-departmental-compliance-at-cerevel/index.html)

“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

[Watch video](/content/customer-stories/roche-powers-digital-transformation-with-veeva-vault-rim/index.html)

###### 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**\
\

### Interested in learning more?

[Contact Us](/content/contact-us/index.html) [Download Product Sheet](/content/wp-content/uploads/2023/07/Veeva-Product-Sheet-Regulatory.pdf?1/index.html)