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Medical Device Regulation training

Medical Device Regulation training
from 4 to 360h flexible workload
valid certificate in your country

What will I learn?

This training provides a practical overview of EU MDR 2017/745 focused on Class IIb wearable cardiac monitors. You will learn to align your QMS with ISO 13485 and ISO 14971, develop compliant technical files, handle software and cybersecurity, conduct clinical evaluations and PMCF, set up PMS and vigilance, and prepare for audits with immediately applicable tools.

Elevify advantages

Develop skills

  • Build MDR-ready QMS: align ISO 13485, PRRC role, and audit preparation.
  • Create MDR technical files: GSPR mapping, UDI, EUDAMED, and Class IIb evidence.
  • Develop clinical evaluation: CEP, CER, performance data, and PMCF for wearables.
  • Apply ISO 14971: run risk analyses, define controls, and close the PMS feedback loop.
  • Manage software and cybersecurity: IEC 62304, threat controls, and cloud suppliers.

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

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EmersonPolice Investigator
The course was essential to meet the expectations of my boss and the company where I work.
SilviaNurse
Very great course. Lots of rich information.
WiltonCivil Firefighter

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