Built for Speed & Compliance.
Proven for MedTech Success.
Bringing a medical device to market can be complex, involving strict regulations, detailed documentation, and careful risk management. QuickVault by Veeva simplifies the process, offering catered solutions built to accelerate MedTech success.
Purpose-Built Solutions for MedTech
Switch from Paper
Drowning in paper? Reduce clutter and increase productivity by switching to an eQMS purpose-built for MedTech.
Remain Audit Ready
Ensure audit-readiness and compliance, so you are prepared and stress-free when regulatory authorities come knocking.
Prepare and Track Regulatory Submissions
Gain full visibility and control over your submission workflows, so you can move faster, reduce risk, and get products to patients sooner.
Automate Design Controls and Reduce Risk
Manage your entire design and development process in an automated, fully validated environment, eliminating compliance risks from day one.
Bring Medical Devices to Market Faster
Eliminate compliance burdens, enhance internal and external collaboration, and accelerate your go-to-market journey for commercial success.
Frequently Asked Questions for MedTech Companies
How does QuickVault support medical device companies?
QuickVault unifies design, regulatory, and production processes into a single platform, helping medical device teams streamline compliance, accelerate market entry, and scale operations efficiently. Every step is supported by built-in FDA, ISO, and GxP best practices, so you can move quickly without risking quality.
How does QuickVault help IVD companies manage ongoing compliance?
IVD companies face constant regulatory updates and growing expectations for traceability. QuickVault simplifies compliance by centralizing documentation, automating version control, and providing structured workflows for design, quality, and submissions. This helps IVD teams stay audit-ready while keeping development timelines on track.
Is QuickVault suitable for startups with limited compliance experience?
Yes. QuickVault is purpose-built for MedTech startups and growing teams. The platform is pre-validated and ready to use from Day 1, with pre-built templates, guided workflows, and expert support to help teams achieve compliance—even without prior regulatory expertise.
Will QuickVault scale as my business grows?
Absolutely. QuickVault is designed to grow with you. Whether you’re launching your first device or expanding your product line globally, the platform adapts to support increasing complexity—without slowing you down.
The platform scales alongside your team, and our flexible subscription model ensures you always have the right level of support—without being locked into long-term contracts.
How does QuickVault reduce submission and approval delays?
QuickVault removes the guesswork from regulatory submissions by automating document management, ensuring version control, and providing submission tracking tools—so you can prepare faster, respond to inquiries quickly, and reduce the risk of costly delays.
Can QuickVault support different regulatory requirements across markets?
Yes. QuickVault is built to meet FDA, ISO, and GxP standards while also offering configurable workflows to support regional variations. Whether you’re preparing a 510(k), CE Mark submission, or aligning with MDR/IVDR, QuickVault ensures your quality and regulatory processes stay compliant.
How do I get started with QuickVault?
Getting started is simple. QuickVault is Day-1 ready, meaning there’s no lengthy implementation process, customization project, or hidden setup fees. You can be up and running in days—not months—saving valuable time and resources when it matters most.
Plus, our flexible, cost-effective subscription model has no long-term commitments, so you get the platform you need now, with the freedom to adjust as your company grows.
Accelerate Your Path to Market 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.