September 16-18, 2018
Philadelphia, PA

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2018 Veeva Global R&D Summit

Veeva Global R&D Summit is an annual gathering of pharma and biotech leaders in clinical, regulatory, quality, and IT. The event is complimentary for Veeva customers and select invited guests.

Over 1,000 life sciences leaders and experts will gather at Veeva Global R&D Summit. The 2017 Global R&D Summit agenda included more than 45 sessions featuring customer case studies in clinical operations, regulatory information management, and quality management. Key topics included:


  • Unifying clinical operations with Vault CTMS and Vault eTMF.
  • Inspection-readiness advice and best practices.
  • Integrating metrics to drive operational efficiency and TMF quality.
  • Accelerating EC and competent authority approvals for faster study startup.
  • Quality and Manufacturing

  • Cloud applications: Risk-based approach to change control and validation.
  • Enabling compliant outsourced manufacturing and contractor collaboration.
  • Learning management: Moving from compliance to performance.
  • Leveraging metrics to drive quality and compliance.
  • Regulatory

  • Bringing visibility to submission authoring and compilation.
  • Best practices for managing correspondence and commitments.
  • Aligning headquarters and affiliates to optimize regulatory processes.
  • Eliminating today’s manual tracking spreadsheets.
  • Tracing documents from origin to multi-market use.
  • Veeva Vault Platform

  • Best practices on configuring Vault applications.
  • Speeding implementation with Vault accelerators.
  • Workshop: How to identify opportunities for Vault Platform.
  • Success stories: Customer-configured solutions.
  • Highlights from 2017 Veeva Global R&D Summit