LexisNexis Reed Tech
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WHITEPAPER
EUDAMED Compliance:
A Practical Guide for 2025
With the UDI/Device Registration module in the EU’s EUDAMED database expected to begin mandatory product reporting in January 2026, the window to prepare is rapidly closing.
Is your organization ready to meet the new UDI and regulatory data submission standards?
Download our free whitepaper to get a step-by-step roadmap to compliance — designed specifically for medical device manufacturers, regulatory teams, and RA/QA professionals navigating the complexities of EU MDR/IVDR.
What You’ll Learn:
- Key deadlines and what they really mean for your business
- How to audit, structure, and format your UDI and regulatory data
- Options for machine-to-machine (M2M) integration
- Managing legacy device data and cross-border requirements
- Internal audit strategies to ensure you’re inspection-ready
- How to avoid bottlenecks, budget delays, and compliance gaps
Plus: EUDAMED Readiness Checklist
Use our expert-designed checklist to assess your organization’s preparedness across data, systems, processes, and people.
Don’t risk missing the 2026 deadline.
Fill out the form to access your free whitepaper and checklist today.