Statements (59)
Predicate | Object |
---|---|
gptkbp:instance_of |
gptkb:software
|
gptkbp:collaborations |
external stakeholders
|
gptkbp:developed_by |
gptkb:computer
|
gptkbp:enables |
data sharing
cross-functional collaboration |
gptkbp:enhances |
stakeholder engagement
data visibility |
gptkbp:facilitates |
knowledge sharing
clinical trials stakeholder feedback |
gptkbp:features |
workflow automation
|
https://www.w3.org/2000/01/rdf-schema#label |
Veeva Vault Medical Affairs
|
gptkbp:improves |
operational efficiency
|
gptkbp:includes |
analytics tools
|
gptkbp:integrates_with |
gptkb:Veeva_CRM
|
gptkbp:is_accessible_by |
gptkb:smartphone
|
gptkbp:is_available_in |
multiple languages
|
gptkbp:is_compatible_with |
FDA regulations
various file formats |
gptkbp:is_designed_for |
medical affairs teams
life sciences industry |
gptkbp:is_designed_to |
streamline processes
|
gptkbp:is_integrated_with |
CRM systems
other Veeva products |
gptkbp:is_optimized_for |
regulatory environments
|
gptkbp:is_part_of |
gptkb:Veeva_Vault
gptkb:Veeva_Vault_Suite Veeva's cloud offerings |
gptkbp:is_scalable |
large enterprises
|
gptkbp:is_supported_by |
gptkb:railway_line
|
gptkbp:is_used_by |
biopharmaceutical companies
|
gptkbp:is_used_for |
content management
content approval |
gptkbp:is_utilized_in |
regulatory submissions
clinical development medical science liaisons |
gptkbp:offers |
gptkb:Database_Management_System
customizable workflows user-friendly interface document management |
gptkbp:offers_courses_in |
best practices
|
gptkbp:provides |
real-time updates
audit trails collaboration tools secure access version control compliance tracking |
gptkbp:provides_access_to |
medical information
|
gptkbp:supports |
data analysis
data integrity regulatory compliance content review processes medical communications |
gptkbp:target_market |
gptkb:drug
|
gptkbp:technology |
gptkb:theorem
|
gptkbp:theme |
medical documents
|
gptkbp:track |
medical inquiries
|
gptkbp:bfsParent |
gptkb:computer
|
gptkbp:bfsLayer |
3
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