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UDI/MDR training

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

What will I learn?

This UDI/MDR Training offers a practical guide to EU-MDR labelling and UDI for complex devices like reusable Bluetooth-enabled infusion pumps. You will learn legal requirements, risk classification, essential label and packaging content, IFU and electronic info rules, usability and risk controls, plus UDI/EUDAMED data and workflows to ensure your documentation is fully compliant, traceable, and ready for inspections.

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 quickly.
  • Learn to write clear, localised IFU and e-IFU that meet Annex I standards.
  • Design risk-based labels with warnings, symbols, and IFU content to prevent misuse.
  • Ensure compliance for Bluetooth devices by aligning software, connectivity, and cybersecurity labels.

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 say

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

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