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EU IVDR Training Courses on the European In Vitro Diagnostic Regulation (2017/746)

Comply Guru offer EU IVDR Training that is available in multiple formats from eLearning, Blended Learning or Instructor-led Learning to help you or your organization learn about new European In Vitro Diagnostic Regulation (2017/746). We were the first training provider to offer Exemplar Global Certified EU IVDR Training in the world…

The European In Vitro Diagnostic Regulation (2017/746) is the new legislation applicable to IVD medical devices being placed on the EU market. The IVDR replaces the EU In Vitro Diagnostics Directive (IVDD) 98/79/EC.

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

WHAT'S NEW

2025 Training Guide

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

2025 Training Guide

Find Your Course

Advanced EU IVDR Practitioner

Medical Devices

Advanced EU IVDR Practitioner

40hrs
EU IVDR Training for Practitioners

Medical Devices

EU IVDR Training for Practitioners

24hrs Exemplar Global Cretified Course
EU IVDR Auditor Training

Medical Devices

EU IVDR Auditor Training

20hrs
PRRC for Medical Devices

Medical Devices

PRRC for Medical Devices

5hrs
EU IVDR 2017/746 Essentials

Medical Devices

EU IVDR 2017/746 Essentials

2hrs
Authorized Representative Training

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.

New Courses to Reach New Heights in 2025
New Courses to Reach New Heights in 2025
Eoin discusses the exciting new courses Comply Guru has launched in 2025 for QARA Professionals within MedTech....
Comply Guru Sponsors Global Access 2024
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....
Why does CAPA get a bad rap in the Medical Device 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....

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CQI & IRCA Approved Training Provider

CQI & IRCA Approved Training Provider

Offering certified courses since 2019

Exemplar Global Recognized Training Provider

Exemplar Global Recognized Training Provider

Offering certified courses since 2020