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

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.
Veeva Submissions
A content management application used to plan, author, review, and approve regulatory submissions.
Veeva Submissions Publishing
Produces compliant published submissions ready to send to global health authorities.
Veeva Submissions Archive
Provides storage, navigation, and search of submitted regulatory applications and related correspondence and questions.

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

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.
Quality-RIM Connection
Shortens the overall timeline from change control event creation to implementation.
RIM–PromoMats Connection
Integrates compliance package generation for direct publishing to health authorities.

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