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UDI/MDR training

UDI/MDR training
flexible workload from 4 to 360h
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. 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 fast.
  • 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.
Workload: between 4 and 360 hours

What our students say

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

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