TrialVault EDC Platform

I-Clindatacrest Clinical Data Management services

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TrialVault EDC Platform
eTMF

TrialVault gives sponsors and CROs a structured pathway from study setup to controlled delivery. It brings together specification-led setup, study build governance, data review visibility, migration readiness, auditability and validation-aware documentation in one coherent service model.

Key capabilities:
- Study build and publish governance
- Sponsor-facing eCRF, EDC configuration and edit-check specifications
- Role-scoped access, auditability and reviewable change history
- Migration readiness, dry-run reconciliation and UAT planning
- Controlled automation with human accountability
- Transparent dashboards for setup progress, open actions and readiness signals

Why review TrialVault with I-ClinDataCrest:
- Platform support paired with experienced clinical data management delivery
- Validation-aware language from early review
- Sponsor oversight through dashboards, review queues and controlled exports
- Flexible UK and India support for responsive study timelines

TrialVault discussions are positioned for walkthroughs, pilots, UAT planning and enterprise-readiness review. Final production-use, validation, certification or regulatory-compliance claims should be confirmed against approved evidence and project-specific requirements.