Medical Device Regulation Law training
Gain expertise in EU MDR for orthopedic implants and more. Cover device classification, clinical evidence needs, supplier agreements, German liability rules, and post-market tasks to cut legal risks, safeguard patients, and ensure market compliance.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
This training offers a practical look at MDR rules, focusing on orthopedic implants and Germany. Cover device qualification, classification, clinical evidence, supplier and quality deals, post-market surveillance, vigilance, and liability risks, then create a solid plan for compliant market entry.
Elevify advantages
Develop skills
- Master MDR classification for orthopedic implants confidently.
- Plan clinical evidence like CER, PMCF, and studies to meet MDR standards.
- Draft supplier contracts covering quality, liability, and MDR obligations clearly.
- Set up efficient post-market surveillance, vigilance, and EUDAMED systems.
- Navigate German liability laws including ProdHaftG, BGB, and authority requirements.
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
Your classes are perfect. I purchased the one-year package and finally have the opportunity to follow various topics of my interest without needing to change platforms... I thank you for everything you do, I've already recommended you to other people...

Giulio CarloDigital Marketing Student
I like how the lessons are straight to the point and how I can switch chapters and skip content I don't need.

Mariana FerresPhotography Student
I like the content and the way videos are presented and transcribed, which speeds up the process!

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The platform is fast, simple to use. The diversity of content and complementary videos help a lot with learning.

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