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Accelerate site activation
Stay inspection ready
Manage trials end-to-end
Pay clinical research sites faster
Streamline and automate training
Improve patient experience
Experience seamless data flow
Automate information sharing
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Aggregate and clean study data
Randomization and supply management
Track global registrations
Plan and manage submissions
Publish to health authorities
Access submissions history
Gain control of GxP documents
Manage and execute paperless validation
Deliver right content to the right station
Ensure role-based qualification and compliance
Access accredited eLearning courses
Manage all quality processes in one place
Simplify postmarket surveillance for medical devices
Optimize QC labs for real-time batch release
Mitigate risk with oversight
Manage safety content
Manage signals from detection through risk evaluation and mitigation
Advance scientific exchange across channels
Centralize & scale medical content
Automate medical inquiry intake & fulfillment
Identify the right experts, plan engagement & measure scientific awareness
Seamless engagement across channels
Events software & services
Faster territory design & alignments
Clean, standardized customer MDM
Compliant content at scale
Data science & analytics platform
Measurement, targeting, & insights with Veeva Crossix
Delivers accurate data, faster
Insights on key people with Veeva Link
High quality data for U.S. life sciences
One place to work with your sponsor
Stay compliant without the effort
R&D, medical, and commercial solutions
Solutions from clinical to commercial
Tailored applications for animal health
Streamline content and data management
Quality and regulatory across brands
Applications to keep innovation compliant
Quality, regulatory, and claims applications
Commercial Summit, Europe
Madrid • November 28-30, 2022
Commercial Summit, North America
Pre-Register • May 2-3, 2023
R&D and Quality Summit, Europe
Sessions On Demand
R&D and Quality Summit, North America
Boston • September 12-14, 2023
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