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EU MDR Training (2017/745) Courses

Comply Guru offer courses that are more convenient, flexible, and effective way to learn about the new European Medical Device Regulation (2017/745).

 

EU MDR Training (2017/745) Courses

EU MDR

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.

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Training Guide

Comply Guru Training Guide 2024
Showing 4 Courses

EU MDR Auditor Training

This course will provide learners with the knowledge and skills required to perform audits of medical device quality management systems (MD-QMS) against the European Union’s Medical Device Regulation (EU 2017/745) in accordance with ISO 19011 and ISO 17021 as applicable.

24 hours Blended Blended Exemplar Global

£ 1195.00

EU MDR Training for Practitioners

This course takes you through the new European Medical Device Regulation (2017/745) , not just from an industry perspective, but also from a Notified Body perspective. It has been specifically designed for Quality & Regulatory Professionals who are new to the Regulation.

20 hours eLearning eLearning CQI & IRCA

£ 995.00

Authorized Representative Training

This course provides clarity on the role and responsibilities of the Authorized Representative under Article 11 and Article 12 of the Medical Device Regulation (MDR) and In Vitro Diagnostics Regulation (IVDR).

7 hours Instructor-led Learning Instructor-led Learning Comply Guru

 

EU Regulations Essentials

Comply Guru offer European Regulation Essentials Courses for organizations looking for a concise, high-level introduction for their staff.

2 hours eLearning eLearning Comply Guru

 

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CQI & IRCA Accredited Training Provider

CQI & IRCA Accredited Training Provider

Offering certified courses since 2019

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Exemplar Global Recognized Training Provider

Offering certified courses since 2020