Regulatory Submission Management Software for MedTech
Accelerate Regulatory Submissions from Planning to Approval
Effectively manage every part of your submission process, from initial planning to final clearance or approval in one connected platform.
Create and Track Regulatory Submissions With Ease
QuickVault gives MedTech teams a faster, smarter way to manage regulatory submissions. Easily compile and maintain accurate submissions using a collaborative builder, automatic file linking, and built-in version control. Regulator interactions are streamlined through an integrated tracker, helping reduce delays and accelerate approvals across global markets.
Streamline Submissions. Shorten Review Times. Accelerate Commercialization.
QuickVault makes your team efficient, automates submission creation, and keeps your medical device product launch on track.
Real-Time Submission Collaboration
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Create global submissions with ease using the submission builder
tool in QuickVault -
Directly connect design control documents and data such as DV&V
records, into the submission - Export the submission in an organized folder structure, prepared for the FDA eSTAR submission portal or for submission to Notified Bodies
Track Regulatory Agency Interactions
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Manage feedback and questions from regulatory authorities with the
submission tracker tool - Reduce response times to submission deficiencies
- Reach approval or clearance faster by avoiding review delays
Built-In Compliance Tools
- Automated traceability, e-signatures, and validation
- Live compliance checks to catch issues early on
- Remain audit ready for future on-site inspections
Smarter Regulatory Submissions for MedTech Teams
The QuickVault by Veeva Difference
QuickVault by Veeva’s purpose-built solution helps MedTech teams accelerate regulatory submissions from initial planning to approval.
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.
Ready to Streamline Your Next Submission?
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.