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UDI/MDR training

UDI/MDR training
from 4 to 360h flexible workload
valid certificate in your country

What will I learn?

UDI/MDR Training provides a focused, practical guide to EU-MDR labelling and UDI for complex devices like reusable, Bluetooth-enabled infusion pumps. 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 so your documentation is compliant, traceable, and inspection-ready.

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 the workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.
Workload: between 4 and 360 hours

What our students are saying

I was just promoted to Intelligence Advisor for the Prison System, and the course from Elevify was crucial for me to be the chosen one.
EmersonPolice Investigator
The course was essential to meet my boss's and the company's expectations.
SilviaNurse
Really great course. Lots of valuable information.
WiltonCivil Firefighter

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