Engineered for Connected, Compliant Research Vault delivers secure, scalable platforms that safeguard data integrity while streamlining compliance processes.
DhatuVault centralizes all clinical trial documentation in a single portal, providing inspection-ready controls for approvals and secure access management across the entire study lifecycle. The platform enforces rigorous role-based permissions for sensitive materials, maintains complete audit trails of every action, and automates approval workflows—delivering 21 CFR Part 11 compliance and regulatory readiness at every phas.
Follow a secure, structured path for managing compliance—empowering teams to control documentation, approvals, and audit readiness with confidence and transparency at every stage.
Easily submit files through our encrypted platform, ensuring data privacy from the start.
Intelligent algorithms sort, tag, and verify your documents for accuracy and compliance.
Collaborate with your team and maintain detailed logs for full audit transparency.
Get real-time insights into compliance status and system health through intuitive dashboards.
Collaborate with your team and maintain detailed logs for full audit transparency.
Easily submit files through our encrypted platform, ensuring data privacy from the start.
Sponsors, CROs, Research sites, and Labs collaborate seamlessly with DhatuVault
Sponsors drive the vision and execution of clinical trials across the globe. DhatuVault provides sponsors with a centralized platform for monitoring complex studies, ensuring regulatory compliance, and making data-driven decisions in real time.
CROs
Labs
Sites
Sponsors drive the vision and execution of clinical trials across the globe. DhatuVault provides sponsors with a centralized platform for monitoring complex studies, ensuring regulatory compliance, and making data-driven decisions in real time.
CROs
Labs
Sites
Regulatory-first architecture, AI-driven automation, and intelligent solutions DhatuVault delivers secure, scalable, and inspection-ready trial management.
Built for global regulatory standards, DhatuVault ensures your trial data is secure, auditable, and inspection-ready.
DhatuVault's AI-powered automation classifies, validates, and manages trial documents reducing manual effort.
Monitor trials in real time with DhatuVault's interactive dashboards providing instant insights.
DhatuVault built by clinical operations experts who recognized the need for intelligent, faster trial documentation management. Today, DhatuVault empowers life sciences teams with solutions that eliminate complexity and accelerate medical breakthroughs.
Trusted by leading life sciences organizations globally to securely manage critical trial documentation with confidence. Our intelligent CTMS combines industry expertise with advanced technology to deliver solutions that ensure regulatory compliance, user-friendliness, and enterprise-scale capabilities.
Faster document turnaround
Lower compliance risk
Higher TMF completeness
Documents processed monthly
System Uptime
Enforces regulatory rigour with automated compliance controls
Real-time trial monitoring, intelligent automation, and instant visibility
Delivers Design, Operate, Govern, and Integrations for trials
DhatuVault delivers complete traceability and regulatory audit readiness alway
Simplifies protocol design and eTMF configuration for faster startup
DhatuVault exceeds regulatory requirements with global certifications and encrypted data protection
Electronic records and signatures meet FDA standards for trustworthiness
Ensures data integrity and system validation for GxP-regulated environments
DhatuVault maintains ISMS certification ensuring information security management excellence
Maintains GDPR compliance for EU data protection and global privacy requirements
