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EU MDR Training Courses on the European Medical Device Regulation (2017/745)

Comply Guru offer EU MDR Training that is available in multiple formats from eLearning, Blended Learning or Instructor-led Learning to help you or your organization learn about the European Medical Device Regulation (2017/745). We were the first training provider to offer IRCA Certified EU MDR Training in the world…

The European Medical Device Regulation (2017/745) has replaced the Medical Devices Directive (93/42/EEC) as the legislation detailing the requirements that manufacturers must meet to place medical devices on the market in the European Union.

Comply Guru offer several types of EU MDR training courses depending on the target audience and/or learning objectives.

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2025 Training Guide

Innovation Leaders for ISO Standards, Auditing & Medtech QA/RA Training

Find Your Course

Medical Devices

EU MDR Auditor Training

24hrs

Medical Devices

Advanced EU MDR Practitioner

40hrs

Medical Devices

EU MDR Training for Practitioners

24hrs

Medical Devices

Post Market Surveillance (PMS) under EU MDR 2017/745

16hrs

Medical Devices

Clinical Evaluation under EU MDR 2017/745

7hrs

Medical Devices

PRRC for Medical Devices

5hrs

Medical Devices

EU MDR 2017/745 Essentials

2hrs

Medical Devices

Authorized Representative Training

4hrs

Read, Watch & Discover More

Our team has you covered with expert insights & updates to stay on top of the latest updates, trends, and changes in the industry.

Why does CAPA get a bad rap in the Medical Device Industry?

Michelle Keane discusses CAPA in Medical Devices including potential reasons organizations struggle and the FDA raise so many findings in this area....

As per ISO 13485, is Spreadsheet Validation required?

As per ISO 13485, is it true or false that a medical device organization that uses spreadsheets is only required to validate spreadsheets that contain...

Comply Guru Sponsors Global Access 2024

Comply Guru proudly sponsored Global Access 2024 which is 's largest conference for Quality and Regulatory Affairs Professionals in Medical Devices....

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Offering certified courses since 2019

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Offering certified courses since 2020