About Veeva Summit
We’re hosting Veeva R&D and Quality Summit as an online experience on October 13-14 to connect the industry while prioritizing the safety of our community.
This Veeva Summit will be a unique experience with new content and participants from across the industry:
- Keynote session with FDA
- New lineup of customer sessions
- Sposor-led small group roundtables
- First look at innovative Veeva Vault capabilities
- Q&A with product experts
- Networking opportunities with 3,000+ peers
For a taste of what’s to come at the October Summit, you can find brief highlights from the regulatory track of Veeva Summit, Europe, held online in May, 2020.
Novo Nordisk's Agile RIM Implementation Accelerates Rollout and Business Value
Michael Buch-Hansen, Project Director
Lars Westergaard Luxhøj, Sr. Project Manager
For Novo Nordisk, the need to replace aging technologies created an opportunity to transform regulatory affairs. Their goal was to create a more connected IT environment while also streamlining regulatory operations, and they chose the Veeva Vault RIM platform to help get them there.
GE Healthcare Streamlines Global Regulatory Processes
James Hendry, Head of Global Regulatory Operations
GE Healthcare Pharmaceutical Diagnostics
GE Healthcare’s pharmaceutical diagnostics division launched Vault Registrations, Vault Submissions, and Vault Submissions Archive in 2019 to improve visibility and confidence in their regulatory data.
Register now for these and more regulatory track sessions:
Regulatory Transformation Fireside Chat
A top-20 pharma details its multi-year journey to transform global operations. Learn how to:
- Set the right goals
- Align teams
- Rethink regulatory processes
- Ensure program success
Building a Connected RIM Experience
An innovative biopharma explores how it successfully implemented Vault RIM in a phased approach. Learn how to:
- Plan a migration
- Transform health authority interaction management
- Connect departments and processes across the organization