See recent enhancements to the RIM-Clinical Operations Connection, accelerating submissions and improving TMF completeness through seamless sharing of product data, study data, and documents across regulatory and clinical. With automatic transfer of key regulatory submission-tracking data to Veeva Study Startup, teams can initiate site activities faster and eliminate manual entry.


Join us live for:


  • RIM-Clinical Operations Connection overview and roadmap
  • Demonstration of submission tracking
  • Live Q&A with product experts

Speakers

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Lucas Alcover

Senior Manager, Development Cloud Strategy
Veeva Systems

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John Tanner

Senior Product Manager, RIM Connections
Veeva Systems

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Eva Santos Garcia

Product Expert, Registrations
Veeva Systems

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Sydney Van Acker

Product Expert, Veeva eTMF & Study Startup
Veeva Systems