Product Registrations
Track and manage product registrations across multiple global markets with status monitoring and renewal tracking. Maintain a centralized registry of all regulatory approvals, clearances, and registrations to ensure your market access is always current.
Key Capabilities
What you get with the Product Registrations module.
See Regulatory Affairs in action
Watch how MoniDoseQMS handles regulatory affairs workflows end-to-end.
Regulatory
Regulatory affairs
What you need for market access: technical documentation, GSPR checklists, declarations of conformity, UDI, EUDAMED and submissions.
Regulatory
Clinical and post-market
Clinical evidence and post-market follow-up: literature reviews, clinical evaluation, PMS, PMCF and PSUR.
How It Connects
Product Registrations doesn't work in isolation. It connects seamlessly with other modules in MoniDoseQMS for full traceability across your quality system.
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Book a 30-minute demo tailored to your regulatory needs. Our team will walk you through how Product Registrations works within your specific compliance context.
More in Regulatory Affairs
Explore other modules in the Regulatory Affairs category.
UDI Records
Manage Unique Device Identification records and ensure compliance with FDA UDI Rule, EU MDR UDI requirements, and other global UDI mandates. Maintain accurate device identifier data and keep your UDI database submissions current across all required markets.
GUDID Submissions
Prepare and track submissions to the FDA Global Unique Device Identification Database. Keep your device listing data accurate and complete, then upload to GUDID yourself and record the submission here. There is no direct API submission.
Declarations of Conformity
Create, manage, and maintain EU Declarations of Conformity as required by EU MDR Article 19. Ensure your DoC documents are complete, accurate, and updated whenever changes affect conformity, with templates that cover all required elements.
CE Marking Procedures
Document and manage your CE marking conformity assessment procedures aligned with EU MDR Annex IX-XI. Track conformity assessment routes, notified body interactions, and ensure all prerequisites are met before applying the CE mark to your devices.
Essential Requirements
Demonstrate compliance with EU MDR Annex I General Safety and Performance Requirements through structured checklists and evidence mapping. Maintain a living GSPR checklist that links each requirement to supporting evidence in your technical documentation.
Technical Documentation
Compile and maintain technical documentation files as required by EU MDR Annex II and III. Organize all required elements including device description, design information, risk management, and clinical evidence in a structured format ready for notified body review.