Would you like to visit a Veeva site closer to you?
Regions
USA
Europe
China 中国
Japan 日本
Asia Pacific
Korea
Latin America
Industries
Life Sciences
Medical Devices
Consumer Goods
Chemical
Cosmetics
Collect and verify site data
Speed trial coding
Aggregate and clean study data
Accelerate site activation
Stay inspection ready
Manage trials end-to-end
Pay clinical research sites faster
Automate information sharing
Overview for sponsors and CROs
Overview for research sites
Track global registrations
Plan and manage submissions
Publish to health authorities
Access submissions history
Manage global quality processes
Simplify postmarket surveillance for medical devices
Improve quality and compliance
Enable shop floor efficiency
Automate training management
Mitigate risk with oversight
Manage safety content
Automate case intake with AI
Manage signals from detection through risk evaluation and mitigation
Engage stakeholders across channels
Access real-time oncology profiles
Scientific content and inquiry management
Delivers accurate data, faster
A single, customer master record
Life sciences-specific data warehouse
Marketing measurement, targeting & insights
Hear from leaders driving launch success
Seamless engagement across channels
Software & services for live & virtual events
Speakers bureau services
Faster alignments and activity planning
Compliant content and digital assets
Go paperless and enable remote monitoring
Connect and scale your research
Run paperless, patient-centric trials
Accelerate study cycle times
Real-time inspection readiness
Unify clinical information & process
Unify registration tracking
Streamline submission planning
Quickly access submissions history
Improve adherence & compliance
Global process management
Simplify post-market surveillance
Streamline training & ensure compliance
End-to-end content management
Global repository for collaboration
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
Veeva R&D and Quality Summit, North America
Oct 15 - Nov 13, 2020
Medical Device & Diagnostics Summit
October 28-29, 2020
Commercial & Medical Summit, Europe
November 17-18, 2020
Veeva R&D and Quality Summit, Europe
May 18-19, 2021
Vault EDC
Vault Coder
Veeva CDB
Vault CTMS
Vault eTMF
Vault Study Startup
Vault Payments
Vault Site Connect
SiteVault
Vault Registrations
Vault Submissions
Vault Submissions Publishing
Vault Submissions Archive
Vault Platform
Vault QMS
Vault Product Surveillance
Vault QualityDocs
Vault Station Manager
Vault Training
Vault Safety
Vault SafetyDocs
Vault Safety.AI
Vault Signal
Demo Center
Oncology Data
Medical Content
Medical CRM
Multichannel CRM
Events Management
Territory Alignment
Customer Reference Data
Master Data Management
Review & Approval + DAM
Commercial Data Warehouse
Crossix Marketing Analytics
Pharma & Biotech
Consumer Health
Animal Health
Medical Devices & Diagnostics
Consulting Services
Training Services
Support & Community
North America
China
Japan
Global Management
Board of Directors
Generation Veeva
Engineering and Product Management
Open Positions
Services
Technology
Agency
CROs
Data
Press Releases
Press Coverage
