Essentials of European Medical Device Regulatory Affairs

Essentials of European Medical Device Regulatory Affairs
This course will provide a basic, comprehensive overview of regulatory requirements and considerations for medical devices in a relaxed and interactive environment.

: 7 March 2019
Where: Hilton Dublin, Charlemont Place, Dublin 2, Ireland
Time: 10.00-17.00

Course overview 

This course provides an opportunity that on-the-job learning doesn't: network and learn from a variety of experts including your fellow delegates. By attending this course, you will gain a basic understanding of the European medical device regulatory requirements and how to comply with them.

Benefits to delegates

  • Develop a broad understanding of the regulatory affairs profession within the medical devices industry. 
  • Build a network to support the rest of your career
  • Meet and learn from experts in the field   
CPD: This course provides 6 CPD hours upon successful completion

To learn more about why Continuing Professional Development is important, visit our Lifelong Learning page.


The latest version of the programme can be downloaded here.


A speaker from HPRA Ireland will be presenting together with:

Neil Armstrong
- CEO, MeddiQuest Regulatory Affairs Limited 

Suitable for

This course is designed for those:

  • Regulatory affairs professionals who require a comprehensive overview of medical devices 
  • Who work in functions allied to medical device regulatory affairs (such as marketing, medical, quality, packaging and legal)
  • From related professions (law, pharmaceutical manufacturing, marketing and sales, healthcare, administration, project management)
  • Those who work in regulatory authorities and those in the regulatory sector


This course is now full. To be added to the waiting list, please email
Course *fees:
Type Fee
Standard   £360+23%VAT 

Discounted places
A limited number of discounted places are available at the rates below.
Please email us at for a discount code before making your booking.

Those working for regulatory agencies, government agencies or academic institutions 

Those working for charities, patient groups or in full-time education

*VAT, if applicable, is charged at VAT the of 23%

    If you hold a current VAT 56B form, please do not continue your registration online.

    Simply send an email with a copy of your form to who will manage your booking.

Related courses

On-demand webinar: Your Career in Regulatory Affairs - Your First Steps

Next steps

Click here for upcoming CRED-level courses.
Click here for upcoming webinars

Terms and conditions

By booking a place on this course you are agreeing to TOPRA's training terms and conditions
07/03/2019 10:00 - 17:00
Hilton Dublin Charlemont Place DUBLIN 2 IRELAND
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Our policy on photography and video

On occasions, TOPRA takes photographs and videos which may be used to help promote our conferences and courses (both online and in print). By purchasing a ticket to attend this meeting you are confirming that you are aware of this and have no objections to your image or voice appearing in any material issued by TOPRA after the meeting.

However, if for any reason you do not wish TOPRA to use your image or voice please let us know

Recording and photography by delegates is not permitted.