Veeva Vault Study Startup
Veeva Vault Study Start-up accelerates the collection, tracking, and management of study start-up activities and content by bringing together site start-up documents and site initiation activities in a single solution. Seamless interoperability with Veeva Vault eTMF allows sponsors, CROs, and sites to access the same clinical information, simplifying collaboration and increasing efficiency.
With Vault Study Start-up you can speed time to site activation and ensure a single source of truth for all start-up related content and data.
- Speed: Faster time to first patient/first visit.
- Visibility: Real-time reporting and dashboards.
- Control: Promotes efficient, global processes.
INTERACTIVE DASHBOARDS AND REPORTSQuickly translate insight into action. Know what’s required, what’s completed, and what’s needed at all times to get to country and site activation.
GLOBAL WORKFLOWSAutomate the collection, tracking, and review of key study documents, submissions to ethics and other bodies, and site essential documents.
SCALABLE AND COMPLIANTInitiate global studies with confidence. Templates support variations for country and local regulations.
SINGLE SOURCE OF TRUTHImprove collaboration as well as document and site initiation quality. Sponsors, CROs, and sites access the same clinical information. Upload a document or record once and reuse across studies.
REAL-TIME COLLABORATIVE AUTHORINGSeamless integration between Veeva Vault and Microsoft Offline Online provides real-time collaborative authoring and does so in a compliant way.
VISIBILITY INTO STUDY MILESTONESTrack study milestones across trial-related activities and quickly understand the impact of events such as protocol amendments with a line of sight into document versions used in each package.
TIME-SAVING DOCUMENT PACKAGESSend documents and relevant tasks for site initiation and other site milestones within a single package.
DEDICATED CONTRACTS AND BUDGETS WORKFLOWS
Veeva Vault Study Startup Product Brief
Veeva TMF Maturity Model