Bristol-Myers Squibb has selected Veeva Vault Registrations and Veeva Vault SubmissionsArchive, new regulatory solutions to manage registration tracking and submission archiving globally.
 
The Vault RIM suite aims to align regulatory processes worldwide, to help improve speed, agility, and compliance. Vault RIM provides real-time access to submission plans, product registration status, health authority correspondence and commitments, and local market submissions.
 
“Life sciences companies struggle to manage product submissions and registration information around the world,” said John Lawrie, director of Veeva Vault RIM. “Veeva understands the breadth of this challenge and has introduced a unified solution that helps harmonize global operations and provides the visibility organizations need to manage their product portfolio more effectively.”
 
Vault RIM is part of Veeva Vault, the first cloud-based regulated content management platform and suite of applications designed for life sciences.