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About
Built by pharma experts.
Powered by AI.
Founded by a pharmacovigilance expert with 15+ years at Novartis, Vifor, and Organon and a compliance engineer building tools for regulated industries.
Meet the Founders
People who understand
pharma compliance.
Our Mission
Modernize pharma
compliance.
Pharmaceutical companies deserve compliance infrastructure that matches the sophistication of their science validation protocols generated in minutes, evidence collected automatically, and audit readiness maintained continuously.
DueVault brings AI to every step of compliance while maintaining the 21 CFR Part 11 audit trails, electronic signatures, and data integrity your regulators demand.
What we automate
GxP validation protocols (IQ/OQ/PQ/CSV)
Pharmacovigilance adverse events, signals, PSUR
FDA audit preparation and inspection management
CAPA workflows and deviation tracking
Supply chain and cold chain monitoring
Vendor qualification and assessments
Clinical trial compliance and site visits
Continuous monitoring across 12 integrations
Our Values
What drives everything
we build.
Security First
Zero-trust architecture. AES-256 encryption. Your data is isolated, encrypted, and never shared with anyone.
Radical Simplicity
Compliance is complex enough. DueVault makes it elegant connect, automate, and stay audit-ready.
Full Transparency
Every AI answer includes citations and confidence scores. No black boxes you always know why.
Customer Obsession
Built by pharma compliance professionals. Every feature solves a real problem we've experienced firsthand.
Our Journey
From idea to
enterprise platform.
2024
Founded
DueVault founded to bridge AI innovation with GxP regulatory expertise in pharmaceutical compliance.
2024
Platform Launch
Launched with 21 CFR Part 11 validation, AI-powered questionnaires, 12 integrations, and audit management.
2025
Full Pharma Suite
Pharmacovigilance, clinical trials, supply chain, 4 autonomous AI agents, and on-premise deployment.
2025
Enterprise Ready
Air-gapped deployment, customer-managed encryption keys, privacy-preserving vendor assessments, and 9+ frameworks.
Global Coverage
9+ frameworks.
Auto-mapped.
Every integration evidence is automatically mapped to the compliance controls that matter across pharma, healthcare, finance, and technology.
21 CFR Part 11ICH Q10EU GMP Annex 11GDPGAMP 5WHO GxPHIPAASOC 2 Type IIISO 27001
Enterprise
On-premise & VPC deployment
Air-Gapped
No external API calls needed
Private AI
Azure OpenAI private endpoints
Zero-Trust
Complete data isolation