Veeva Vault Registrations

Keep Pace with
Evolving Regulations

Track global product registrations and associated changes.

Announced 2015
Customers 100+

Vault 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 dataoutput (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.

Why Vault Registrations

Plan, track, and report on product registrations

  • 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.

Exceed the
likely outcome


of the top 20 companies use Vault RIM


IT systems consolidated into one


reduction in written standards

  • Atara-Bio Bayer BeiGene GSK Jazz LEO Moderna MundiPharma Novo-Nordisk UCB Vertex


Explore and learn

IDMP readiness center
View resources
Solving pharma’s regulatory jigsaw puzzle
Read ebook
Global submission planning at BMS
View infographic

Interested in learning more about how Veeva can help?