Medical Device Regulation Law training
Gain expertise in EU MDR for orthopedic implants. Cover device classification, clinical evidence needs, supplier agreements, German liability laws, and post-market obligations to cut legal risks, ensure patient safety, and maintain market compliance.

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.What our students say
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