NSAI and Enterprise Ireland Briefing on Medical Device Regulations and Brexit

Introduction

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. 

Speakers

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.

Dublin

27th February, 18:00-20:00

NSAI HQ, Swift Square, Santry,Dublin. 9

Register Now