Statements (79)
Predicate | Object |
---|---|
gptkbp:instanceOf |
software
|
gptkbp:developedBy |
gptkb:Veeva_Systems
|
gptkbp:enables |
document sharing
faster study initiation |
gptkbp:enhances |
data integrity
project management team collaboration collaboration among teams data security stakeholder engagement regulatory processes |
gptkbp:facilitates |
study documentation
collaboration with sites study execution study startup processes |
https://www.w3.org/2000/01/rdf-schema#label |
Veeva Vault Study Startup
|
gptkbp:improves |
operational efficiency
|
gptkbp:includes |
workflow automation
|
gptkbp:integratesWith |
gptkb:Veeva_Vault
|
gptkbp:isAvailableIn |
enterprise use
cloud platform SaaS deployment |
gptkbp:isCompatibleWith |
mobile devices
third-party applications various EHR systems |
gptkbp:isDesignedFor |
streamline processes
streamline workflows support compliance study teams life_sciences_industry |
gptkbp:isFocusedOn |
regulatory compliance
improving efficiency improving timelines study startup efficiency |
gptkbp:isIntegratedWith |
gptkb:Veeva_Vault_Regulatory
gptkb:Veeva_Vault_Clinical gptkb:Veeva_Vault_Quality gptkb:Veeva_Vault_Study |
gptkbp:isPartOf |
gptkb:Veeva_Vault_suite
clinical trial management solutions clinical trial software solutions clinical trial ecosystem clinical trial management ecosystem Veeva_Vault_platform |
gptkbp:isUsedBy |
clinical research organizations
|
gptkbp:isUsedFor |
document control
|
gptkbp:isUtilizedFor |
academic institutions
pharmaceutical companies research institutions biotech companies medical device companies contract research organizations |
gptkbp:offers |
collaboration tools
customizable workflows data analytics training resources cloud-based solutions real-time visibility reporting capabilities data management tools |
gptkbp:provides |
real-time updates
audit trails data visualization secure access user-friendly interface data integrity checks user support document management compliance tracking |
gptkbp:providesAccessTo |
study documents
|
gptkbp:reduces |
administrative burden
|
gptkbp:supports |
regulatory compliance
data sharing data management protocol development regulatory submissions study planning multi-site studies |
gptkbp:usedFor |
clinical trial management
|