Veeva Registrations

Plan, Track, and Report on Product Registrations

Registrations allows sponsors to plan, track, and report on global product registrations along with health authority correspondence and commitments.

Events provide the ability to manage product changes, from the initial assessment of the proposed change through submission creation, health authority interactions, and final registration update. Label changes can be tracked and managed at both the global and local level. Registrations also produces compliant product data output (e.g., xEVMPD and IDMP) for EU regulations.

Dashboards and reports allow personnel to track the progression of change events and provide an understanding of product registration locale.

Announced 2015 Status Mature Customers 100+

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

Learn how Veeva’s flexible data model supports the latest IDMP standards

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 Registrations

Plan, track, and report on product registrations

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Improve data quality

Streamline registration management by reducing data duplicates and discrepancies.

Provide global visibility

Stay informed with a complete view into the marketing status of your global product portfolio.

Speed health authority responses

Manage product registration queries and commitments to stay ahead of response deadlines.

Customer Success

Veeva RIM is trusted by 400+ top and emerging biopharmas

“Decisions that once took days or weeks can now be made within minutes.”

Joe McLaughlin, Head of Regulatory Business Practice and Innovation

Sanofi

“Veeva Registrations provides additional granular detail into our submissions. This visibility saves time and sets us up for global change management.”

Wim DHaeze, Senior Director, Global Regulatory Operations

Sarepta

“A RIM system starts to become a strategic asset for organizations that do it right.”

Matt Neal, Senior Director Regulatory Affairs Operations

Atara

Resources

Explore and Learn

[View Features Brief Veeva Registrations Features Brief\ \ [View Resources The Path to Unified RIM: Key Attributes Driving Regulatory Excellence\ \ [Read eBook Solving Pharma’s Regulatory Jigsaw Puzzle\ \