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Medical Device Regulations (MDR)

July 17

€399

Introduction to the MDR one day training

The legislation outlining the requirements for medical device manufacturers prior to placing them on the market in the European Union is changing. The old Medical Devices Regulation (EU 2017/745) is to be replaced by the Medical Devices Directive (93/42/EEC). The new regulations place greater emphasis on accountability for all players and with greater scrutiny of both clinical evaluation and post-market clinical evaluations and improved traceability of devices for the full life cycle.

Who should attend this training:
Those with a working knowledge QMS from all levels within the organisation including (but not limited to):
• Authorised Representatives
• Manufacturing personnel
• Quality
• Regulatory Affairs
• Design and Development
• Economic Operators for example importers and distributors

Need a quote for in-house training email info@iqc.ie 

or

phone +353 (0) 1-2040646

Tickets

Tickets are not available as this course has passed.

Details

Date:
July 17
Cost:
€399
Courses Categories:
,

Organiser

Philip Byrne

Venue

Dublin
Maldon Hotel Newlands Cross, Naas Road, Newlands Cross
Dublin 22, Co. Dublin D22 V6Y6 Ireland
+ Google Map
Phone:
+35314640140
Website:
https://www.maldronhotelnewlandscross.com/