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NSAI and Enterprise Ireland would like to invite you to attend a briefing on the new medical device regulations and the potential impacts of Brexit on the medical devices sector, taking place in Dublin and Galway. 

This event is relevant for:

  • ‌Medical device manufacturers.
  • ‌Organisations involved in the medical device supply chain.
  • ‌People working in quality and regulatory affairs.

This event will focus on: 

  • Clinical requirements for the medical device regulation.
  • Device classification and product technical file requirements.
  • Quality system requirements.
  • Brexit implications for medical device manufacturers. 


Colm O Rourke Brexit and introduction to medical  device regulation implications a notified body perspective Dublin and Galway

Yvonne Ndefo: Clinical requirements for the Medical device regulation Dublin and Galway

Susan Murphy: Device classification and Product technical file requirements  for the  Medical device regulation Dublin

Tom Costello: Medical  device regulation and quality system requirements  Dublin

Aishling Owens: Device classification and Product technical file requirements for the  Medical device regulation Galway

Niamh Lynch: Medical  device regulation and quality system requirements   Galway

Manus Rooney: Overview of Enterprise Ireland Brexit Supports for SMEs Dublin and Galway

In addition, Enterprise Ireland will be available to provide information on Brexit supports for SME's.​​

Course Locations

This event is complimentary, but on-line booking is required. Places are limited, so early booking is advisable.


27th February, 18:00-20:00

NSAI HQ, Swift Square, Santry,Dublin. 9

Register Now

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25th February, 18:00- 20:00

Galmont Hotel, Lough Atalia road, Galway

Need to get in touch? Email