Design Control & Risk Management Software for MedTech
Automate Design Controls. Reduce Risks. Accelerate Innovation.
Take the burden out of innovation – automate design controls, control risk, and develop medical devices faster with confidence.
QuickVault Automates Design Controls & Reduces Risk
QuickVault empowers MedTech companies to fully automate design controls, reduce risk, and bring medical devices to market faster. With built-in traceability, real-time collaboration, and automatic generation of design and development files, QuickVault simplifies compliance while supporting innovation at every product lifecycle stage.
Manage Design Controls & Risk in One Seamless Workflow
Automated Design Controls
- Manage the whole design control project on a single platform
- Increase team efficiency with automated workflows
- Unify design requirements, risks, specifications, verifications, validations and Design Transfer in a single system
- Manage, document and link Design Reviews and Risk Reviews within the QuickVault product workspace
Stay Above Compliance
- Align with FDA 21 CFR Part 820 and ISO 13485 design control requirements
- Keep audit-ready documentation throughout every design stage
- Get built-in visibility for approvals and changes
Minimize Risks & Project Delays
- Catch issues early on with connected quality and design data
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Reduce risk with marketing submission delays by minimizing data and
document gaps - Focus on innovation and speed - not paperwork or regulatory guesswork
Cut Time to Market With Design Control Automation
The QuickVault by Veeva Difference
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.
Less Risk, More Control 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.