QuickVault by Veeva’s new functionality helps MedTech teams reduce submission timelines, increase accuracy, and maintain alignment from development to approval.
Watch the short video below for a brief introduction to the new functionality.
Centralize submission planning and task execution with real-time visibility, version-controlled documents, and audit-ready traceability—all in one place.
Jumpstart submissions using pre-configured templates for eSTAR, EU MDR/IVDR, IMDRF, and PreSTAR, or customize them to match internal standards.
Automatically compile regulator-ready ZIP files with built-in compliance checks—saving time and avoiding last-minute surprises.
Track and organize all interactions with regulatory bodies like the FDA to stay responsive and audit-ready across regions.
New REG document types and editable master forms improve consistency and reduce duplicate work throughout the draft-to-approval lifecycle.
New navigation and dedicated areas for Marketing and Sales improve cross-functional handoffs as teams move from submission through commercialization.
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 by Veeva gives MedTech companies the visibility and control they need to deliver safe, effective products to patients and succeed at every stage.