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Demo Veeva Registrations Global Content Plans
Veeva Systems Inc   2026-01-15 に公開
  Global Content Plans allows for better document assembly for central teams to local teams, creating more efficient submission management. See how it works in this 6 minut   ...more
Quality Events Agents
Veeva Systems Inc   2026-01-15 に公開
  Aggregate data across multiple objects to generate narrative summaries for Investigations and CAPA plans.   ...more
Improve Safety Oversight and Reduce Risk
Veeva Systems Inc   2026-01-15 に公開
  See how Veeva Safety leverages real-time reports and dashboards and seamless collaboration to provide visibility and compliance for adverse events.   ...more
OpenData Live Demo
Veeva Systems Inc   2026-01-15 に公開
  Provide licensed HCP/HCO data access to non-CRM users. Features advanced search, filters, and cross-functional access for Compliance, Marketing, and more.   ...more
Season 4 Episode 5: ICH E6(R3): Shifting the Paradigm from Process to Purpose
Veeva Systems Inc   2026-01-15 に公開
  In this episode, we pull back the curtain on the monumental effort required to reshape global clinical trial standards. Manny and guests Lisbeth Bregnhoj and Cheryl Grand   ...more
Veeva RIM: End to End Regulatory Solution
Veeva Systems Inc   2026-01-09 に公開
  Veeva RIM is a suite of applications providing fully integrated regulatory information management (RIM) capabilities on a single cloud-based platform including submission   ...more