Device-to-Market Platform For MedTech Success
Designed for MedTech Success. Built for Speed.
Bringing a medical device to market and scaling your business is complex. QuickVault simplifies this process, freeing you to focus on innovation while ensuring compliance, successful regulatory submissions, and robust infrastructure for commercial growth.
Bring Your Medical Device to Market Faster and Scale Your Business With Confidence
Developing a medical device and operating a MedTech company involves complicated and time-consuming regulatory processes. QuickVault simplifies this journey, making it easier than ever to bring your medical device to market and scale your operations.
Accelerate Your MedTech Milestones
QuickVault accelerates your MedTech milestones by eliminating organizational waste and streamlining your path to market.
Design Control Automation
- Manage the design and development project completely within one platform
- Create Design Control items and link with risk management for full control of DV&V activities and associated data
- Populate and export design & development files with a single click
Submission Efficiency
- Build a marketing submission in parallel with Design Control activities
- Create and manage global submissions with ease
- Track and address regulatory authority questions to reduce submission review times
Post-Market Operations
- Manage post-commercial operations such as suppliers and manufacturing
- Address quality events such as NCRs, CAPAs and Complaints with specific workflows allowing for compliance, fast resolution and audit readiness
- Quickly scale your team with streamlined onboarding & training
An eQMS Platform That Moves at the Speed of MedTech
The QuickVault by Veeva Difference
QuickVault by Veeva is designed for MedTech speed. You focus on creating innovative products, and we will guide you through the MedTech journey from concept to commercialization and beyond.
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.
Accelerate Time to Market with a Purpose-Built Solution
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.