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Medical Device Regulation Law training

Medical Device Regulation Law training
flexible workload of 4 to 360h
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 pacts, post-market surveillance, vigilance, and liability risks. Build a solid plan for compliance and safe market entry.

Elevify advantages

Develop skills

  • Master MDR classification for orthopedic implants confidently.
  • Plan clinical evidence like CER, PMCF, and investigations per MDR.
  • Draft supplier contracts aligning quality, liability, and MDR duties.
  • Set up efficient PMS, vigilance, and EUDAMED post-market systems.
  • Navigate German liability under ProdHaftG, BGB, and authority rules.

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

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 Carlo
Giulio CarloDigital Marketing Student
I like how the lessons are straight to the point and how I can change chapters and skip content that I don't need.
Mariana Ferres
Mariana FerresPhotography Student
I like the content and the way of presentation and video transcription, which speeds up the process!
Luciana Alvarenga
Luciana AlvarengaNail Design Student
The platform is fast, simple to use. The diversity of content and complementary videos help a lot in learning.
André Felipe
André FelipePrompt Engineering Student

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