UDI/MDR training
Master EU-MDR and UDI for medical devices in healthcare. Gain skills in labelling, risk classification, IFU creation, UDI/EUDAMED data management, and post-market updates to ensure devices remain compliant, traceable, and safe for patients and clinicians.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
UDI/MDR Training offers a focused, practical guide to EU-MDR labelling and UDI for complex devices like reusable, Bluetooth-enabled infusion pumps. You will learn legal requirements, risk classification, mandatory label and packaging content, IFU and electronic information rules, usability and risk controls, plus UDI/EUDAMED data and workflows to make your documentation compliant, traceable, and ready for inspections.
Elevify advantages
Develop skills
- EU-MDR labelling mastery: apply Annex I, II, III rules to real device labels.
- UDI and EUDAMED skills: build compliant UDI-DI/PI data and register devices quickly.
- IFU and e-IFU writing: create clear, localised, Annex I-compliant instructions.
- Risk-based labelling: design warnings, symbols and IFU content to reduce misuse.
- Bluetooth device compliance: align software, connectivity and cybersecurity labelling.
Suggested summary
Before starting, you can change the chapters and 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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