UDI/MDR training
Gain mastery in EU-MDR and UDI requirements for healthcare medical devices. Cover labelling standards, risk assessment, IFU guidelines, UDI/EUDAMED records, and ongoing updates to ensure devices remain compliant, trackable, and secure for patients and medical staff.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
UDI/MDR Training delivers targeted, hands-on guidance on EU-MDR labelling and UDI for intricate devices like reusable Bluetooth infusion pumps. Master regulatory demands, risk categories, essential label and package details, IFU and digital info standards, usability safeguards, risk mitigation, plus UDI/EUDAMED data processes for fully compliant, traceable, and audit-prepared documentation.
Elevify advantages
Develop skills
- EU-MDR labelling expertise: implement Annex I, II, III guidelines on actual device labels.
- UDI and EUDAMED proficiency: construct compliant UDI-DI/PI records and register devices swiftly.
- IFU and e-IFU creation: produce straightforward, localised, Annex I-compliant manuals.
- Risk-oriented labelling: craft cautions, icons, and IFU details to minimise errors.
- Bluetooth device adherence: synchronise software, links, and cyber protection 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
FAQs
Who is Elevify? How does it work?
Do the courses have certificates?
Are the courses free?
What is the course workload?
What are the courses like?
How do the courses work?
What is the duration of the courses?
What is the cost or price of the courses?
What is an EAD or online course and how does it work?
PDF Course