Statements (62)
| Predicate | Object |
|---|---|
| gptkbp:instance_of |
gptkb:legal_case
|
| gptkbp:bfsLayer |
3
|
| gptkbp:bfsParent |
gptkb:computer
|
| gptkbp:developed_by |
gptkb:computer
|
| gptkbp:enables |
real-time updates
audit readiness |
| gptkbp:enhances |
data integrity
collaboration efficiency |
| gptkbp:facilitates |
collaboration among stakeholders
regulatory submissions |
| gptkbp:features |
search functionality
|
| https://www.w3.org/2000/01/rdf-schema#label |
Veeva Vault e TMF
|
| gptkbp:improves |
efficiency in document retrieval
|
| gptkbp:includes |
version control
|
| gptkbp:integrates_with |
gptkb:Veeva_Vault
|
| gptkbp:is_accessible_by |
gptkb:Cloud_Computing_Service
authorized users |
| gptkbp:is_adopted_by |
CR Os
|
| gptkbp:is_available_in |
multiple languages
|
| gptkbp:is_compatible_with |
FDA regulations
data privacy regulations ICH guidelines other Veeva products |
| gptkbp:is_designed_for |
clinical operations teams
|
| gptkbp:is_designed_to |
streamline processes
|
| gptkbp:is_integrated_with |
project management tools
clinical trial software e-signature solutions |
| gptkbp:is_part_of |
clinical data management
regulatory compliance strategy clinical trial management process Veeva Vault suite |
| gptkbp:is_scalable |
small to large organizations
|
| gptkbp:is_supported_by |
customer service team
|
| gptkbp:is_used_by |
pharmaceutical companies
biotech companies |
| gptkbp:is_used_for |
study start-up
|
| gptkbp:is_utilized_in |
quality assurance
data collection risk management stakeholder communication data management study documentation document review document archiving site management regulatory documentation |
| gptkbp:offers |
customizable workflows
real-time visibility mobile access |
| gptkbp:provides |
data analytics
secure access training resources user-friendly interface document management |
| gptkbp:reduces |
paperwork
time to approval |
| gptkbp:supports |
regulatory compliance
data sharing multiple file formats global trials |
| gptkbp:used_in |
clinical trials
|