# Regulatory Transformation with Unified RIM

End-to-end regulatory information management on a single platform.

[**Learn about IDMP and best practices from BMS and GSK**](/content/products/vault-platform/vault-rim-idmp-resource-hub/index.html)

### Veeva RIM

Veeva RIM unifies regulatory systems and processes on a single cloud platform to enable end-to-end submission and registration management.

RIM applications share a common data model, which allows for regulatory business functions to run in one Vault.

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

[**Veeva Registrations**  
Plans, tracks, and reports on global health authority product registrations and associated changes.](/content/products/veeva-registrations/index.html)  
[**Veeva Submissions**  
A content management application used to plan, author, review, and approve regulatory submissions.](/content/products/veeva-submissions/index.html)  
[**Veeva Submissions Publishing**  
Produces compliant published submissions ready to send to global health authorities.](/content/products/veeva-submissions-publishing/index.html)  
[**Veeva Submissions Archive**  
Provides storage, navigation, and search of submitted regulatory applications and related correspondence and questions.](/content/products/veeva-submissions-archive/index.html)

##### Veeva Falcon for Regulatory

Standard AI agents that do the work for you. Agentic authoring and automated health authority interactions accelerate global submission cycles.

[Learn More](/content/products/falcon/index.html)

### Veeva Connections

Veeva Connections are Veeva-delivered integrations that seamlessly transfer data and documents.

[**RIM–Clinical Operations Connection**  
Enables users to automatically share product, study, and site information.](/content/resources/vault-clinical-operations-to-rim-connection/index.html)  
[**Quality-RIM Connection**  
Shortens the overall timeline from change control event creation to implementation.](/content/resources/streamlining-change-control-and-variation-management/index.html)  
[**RIM–PromoMats Connection**  
Integrates compliance package generation for direct publishing to health authorities.](/content/resources/vault-promomats-to-rim-connection-product-brief/index.html)

###### Demo

### Veeva RIM End-to-End Platform

Veeva RIM provides an authoritative source for regulatory documents and information globally. Content and data converge in a single cloud platform that unifies registration tracking, correspondence and commitments, submission document management, dossier publishing, and regulatory submission archiving.

### Explore and Learn

[**Read Features Brief**  **A Single, Authoritative RIM Solution**  
  
[**Read Blog**  **Modernizing Regulatory Operations with Automation and AI**  
  
[**Watch Video**  **Daiichi Sankyo is Unifying Their RIM Systems to Unify Data and Eliminate Rework**  
  
[**Watch Video**  **Preparing for Regulatory Connections: Best Practices to Ensure Data Quality**