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EU MDR responsible person training

EU MDR responsible person training
from 4 to 360h flexible workload
valid certificate in your country

What will I learn?

EU MDR Responsible Person Training provides clear, practical guidance to perform PRRC duties confidently. Master Article 15 requirements, technical documentation, device release controls, risk management, clinical evidence, post-market surveillance, audits, vigilance reporting, change control, and governance to ensure compliance and support safe devices.

Elevify advantages

Develop skills

  • Apply Article 15 MDR: define PRRC duties, qualifications, and daily decisions.
  • Build compliant MDR technical files and sign device release with confidence.
  • Lead Notified Body audits and respond to findings with robust CAPA evidence.
  • Manage MDR risk, design changes, and clinical evidence for Class IIb devices.
  • Oversee PMS, vigilance, and PRRC governance to protect patients and liability.

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
Workload: between 4 and 360 hours

What our students say

Your lessons 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 I don't need.
Mariana Ferres
Mariana FerresPhotography Student
I like the content and the way videos are presented and transcribed, 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 really help with learning.
André Felipe
André FelipePrompt Engineering Student

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