Modernize Medtech Regulatory with a Single Application
Seamlessly link product data, global submissions, and health authority interactions
Veeva MedTech RIM leverages twenty years of regulatory expertise across hundreds of global implementations and incorporates medtech-specific workflows to support the full device and diagnostic lifecycle.
Unlike Veeva RIM, which supports both device and drug products with four distinct applications - Registrations, Submissions, Publishing, and Archive - Veeva MedTech RIM combines standardized dossier planning, global market filings, and approval workflows into a single application to streamline end-to-end regulatory processes and accelerate market entry.
Built on the Veeva Vault Platform, Veeva MedTech RIM connects to Veeva Quality Cloud and Veeva PLM, providing a single, compliant source of truth across the entire lifecycle, from early design changes to global market filings.
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Attribute-driven workflows
Pre-configured data models tailored to specific regulatory pathways for hardware, IVDs, SaMD, combination products, and capital equipment.
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Agency interactions
Centralized tracking for health authority questions, formal correspondences, and commitments tied directly to submissions
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Unified analytics
Real-time reporting and dashboards across all global registrations, submission milestones, and market data.
Products
Veeva MedTech RIM
With engineered connectivity from R&D and BOM to global registration and ship release, Veeva MedTech RIM eliminates custom APIs and leverages native AI agents to operate securely inside the GxP audit trail.
Granular control
Native SKU and variant-level tracking for complex device families
Device lifecycle
Direct management of UDI, technical files, and regional dossiers
Attribute logic
Tailored workflows for hardware, IVD, SaMD, and capital equipment
Supply chain gate
Automated approval status feeds into ERP for global ship-release control
