Course Description

The Medical Device Regulation (CE Marking Process Key Updates)

The Medical Device Regulation (CE Marking Process Key Updates) is a course run by SQT Training Ltd, Dublin. It is a 'Classroom Based' course with a duration of One day. For more information about The Medical Device Regulation (CE Marking Process Key Updates) at SQT Training Ltd, please review the details below.

The Medical Device Industry is currently transitioning from the Medical Device Directive (MDD) 93/42/EEC to the Medical Device Regulation (MDR) 2017/745. As an industry we need to progress through this transition period in order to keep our products on the European Market and retain our CE mark. It is important therefore that we understand the MDR requirements and the key changes this entails for our products so that we can plan for this change.

This course will look at steps involved in the CE marking process through the MDR (what remains the same, what has changed) as well as other key changes that are required. This course will also link the ISO 13485:2016 quality management system (QMS) requirements to the MDR QMS requirements but emphasizing the importance of the MDR as a legal requirement.

The The Medical Device Regulation (CE Marking Process Key Updates) course at SQT Training Ltd is listed in's national courses finder.
Training ProviderSQT Training Ltd
Course LocationDublin
Course TypeClassroom Based
Course Start Date24th September 2020
Course End Date24th September 2020
Course DurationOne day
Course Time9:00am - 5:00pm
Course FeePOA
Phone+ 00353 61 339040
For more information about SQT Training Ltd, please visit our College page on by clicking here.

Course Provider

SQT Training Ltd

Callan Centre Castletroy, National Technology Park, Various Locations around Dublin, Dublin, Republic of Ireland

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