UDI/MDR training
Gain expertise in EU-MDR and UDI requirements for medical devices in healthcare settings. Master labelling standards, risk classification, IFU development, UDI/EUDAMED data management, and post-market surveillance to keep devices compliant, traceable, and safe for patients and clinicians.

from 4 to 360h flexible workload
certificate valid in your country
What will I learn?
This EU-MDR and UDI training provides a practical guide to labelling and UDI for complex devices like reusable Bluetooth-enabled infusion pumps. Cover legal obligations, risk classification, required label and packaging content, IFU and electronic instructions rules, usability and risk management, plus UDI/EUDAMED data workflows for fully compliant, traceable, and inspection-ready documentation.
Elevify advantages
Develop skills
- Master EU-MDR labelling by applying Annex I, II, III rules to actual device labels.
- Develop UDI and EUDAMED expertise to create compliant UDI-DI/PI data and register devices efficiently.
- Learn to write clear, localised IFU and e-IFU that comply with Annex I requirements.
- Design risk-based labelling including warnings, symbols, and IFU content to prevent misuse.
- Ensure compliance for Bluetooth devices by aligning software, connectivity, and cybersecurity labelling.
Suggested summary
Before starting, you can change the chapters and the workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.What our students say
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