Pass Every Audit with Confidence
Audits are intimidating and consume vast resources to get ready for. Stay prepared and in control with QuickVault.
Remain Audit Ready, At Any Time
QuickVault helps your MedTech company remain audit-ready by keeping your documents and records organized, interconnected, and traceable. Stay prepared for inspections anytime — without the scramble.
How QuickVault Makes Audits Easier for MedTech Teams
QuickVault makes audits easier for MedTech teams by eliminating the chaos of last-minute prep and giving teams complete visibility and control over their quality documents and data. Whether it’s an internal or external audit, MedTech teams can feel confident that they are audit-ready at any time.
Real-Time Record Keeping
- Swiftly create and approve documents in compliance with FDA 21 CFR Part 11
- Easily find and retrieve documents and other quality records
- Maintain a detailed audit trail across the platform
Built-In Compliance Controls
- Ensure every process meets FDA and EU MDR requirements
- Enforce industry best practices with automated workflows
- Reduce the risk of noncompliance with ready-to-use, customizable templates
Automated Traceability
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Easily find related records and documents by leveraging the
“connect everything” functionality within QuickVault - Track changes, approvals and dependencies across the product lifecycle
- Full transparency across the platform, including in-depth audit trails
Regulatory Inspections Without the Last-Minute Prep
The QuickVault by Veeva Difference
QuickVault by Veeva makes regulatory audits a breeze with its ready-to-use, intuitive solution designed to keep you prepared for unexpected inspections.
QuickVault comes fully validated and compliant with 21 CFR Part 11/EU Annex 11.
Compliance is made easy with QuickVault, which is designed to support 21 CFR Part 820, ISO 14971, EU MDR & IVDR, and other global compliance standards.
QuickVault is ready to be used by MedTech teams right away. Unlike competitors, there are no lengthy implementations or customization projects required.
Get started immediately with pre-configured workflows and automated compliance tracking.
Unlike other QMS software, QuickVault was specifically designed with MedTech companies in mind. We focus on one industry and scale with you as your product and business grow.
With industry best practices embedded, QuickVault helps teams control design and documentation, manage quality events, track training, and ensure full compliance with regulations.
Dealing with multiple systems can hold your team back. QuickVault is an all-in-one platform that’s built to support your full product lifecycle journey.
By unifying design, submission, and production in a seamless, scalable platform, QuickVault eliminates inefficiencies, ensures continuous compliance, and helps teams stay agile at every stage.
Simplified Audit-Readiness With QuickVault
QuickVault by Veeva is the leading device-to-market solution for MedTech companies. Built for full device lifecycle support, the platform unifies design, regulatory, quality, and post-commercial operations in one scalable environment—helping teams stay agile, compliant, and ready to grow.
From concept through commercialization and beyond, QuickVault gives MedTech companies the visibility and control needed to deliver safe, effective products to patients and succeed at every stage.