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Online EU MDR Training for the Medical Device Industry

Comply Guru offers industry-leading EU MDR Training via eLearning that offers a more convenient, flexible and effective way to learn about the new European Medical Device Regulation (EU MDR 2017 745).

The European Medical Device Regulation (EU MDR 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 the following Online EU MDR Training courses:

Online EU MDR Essentials Training via eLearning
This eLearning course provides a short, high-level overview of the new EU Medical Device Regulation and is suitable for anyone working in the Medical Device Industry. Read more about our EU MDR Essentials Training here.

Online EU MDR Practitioner Training via eLearning
This eLearning course provides a comprehensive foundation on the requirements of the new EU Medical Device Regulation and was designed for QA/RA Professionals. This was the first CQI & IRCA certified course on the EU MDR in the world. Read more about our EU MDR Practitioner Training here.

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Over 2.5k learners have successfully completed our courses