Veeva Vault RIM

Veeva Vault RIM

Veeva Vault RIM enhances regulatory processes for life sciences, MedTech, and consumer goods on a unified cloud platform. It ensures data integrity and agility throughout submission planning, tracking, and publishing. By centralizing product registration, streamlining compliance, and automating information sharing, it enables efficient coordination across global teams while maintaining oversight and risk management.

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Top Veeva Vault RIM Features

  • End-to-end regulatory management
  • Streamlined submission planning
  • Automated regulatory process steps
  • Comprehensive submissions history
  • Centralized product registration data
  • Real-time compliance tracking
  • Role-based qualification management
  • Continuous publishing process
  • Integration with clinical operations
  • Flexible data model for IDMP
  • Fast and efficient submission delivery
  • Seamless data sharing across teams
  • Automated information sharing capabilities
  • Complete traceability for submissions
  • Centralized medical content management
  • Digitized study monitoring
  • Enhanced oversight for safety content
  • Tailored applications for animal health
  • Real-time batch release optimization
  • Accelerated insights into KOLs.