Medical Device Regulation Law training
Gain expertise in EU MDR for orthopaedic implants and more. Master device classification, clinical evidence, supplier contracts, German liability rules, and post-market obligations to cut legal risks, safeguard patients, and ensure compliant devices stay on the market. This training delivers practical insights with a focus on Germany.

from 4 to 360h flexible workload
certificate valid in your country
What will I learn?
This Medical Device Regulation Law Training offers a targeted, practical overview of MDR requirements, emphasising orthopaedic implants and Germany. Master device qualification and classification, clinical evidence standards, supplier and quality agreements, post-market surveillance, vigilance, and liability risks, then craft a solid compliance and implementation plan for safe, legal market access.
Elevify advantages
Develop skills
- Master MDR classification: confidently classify orthopaedic implants swiftly.
- Plan clinical evidence: swiftly design MDR-compliant CER, PMCF, and investigations.
- Draft supplier contracts: align quality, liability, and MDR duties clearly.
- Set up post-market systems: build efficient PMS, vigilance, and EUDAMED workflows.
- Navigate German liability: manage ProdHaftG, BGB risks and authority actions.
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.What our students say
Your lessons are perfect. I purchased the one-year package and finally have the opportunity to follow various topics of interest without needing to change platforms... I'm grateful for everything you do, I've already recommended you to other people...

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I like how the lessons are straight to the point and how I can change chapters and skip content I don't need.

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

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