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Essentials of European Medical Device Regulatory Affairs




Dublin, Ireland


12 Nov 2020

Reference No: T2006410-TOP

Apply for this event

Key points about this Training Event

  • 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
Event Description

Course Outline:

This course provides an opportunity that on-the-job learning doesn't. By attending this course, you will gain a basic understanding of the European medical device regulatory requirements and how to comply with them.

When & Where?

12 November 2020

Dublin, Ireland


Standard Fee: £360.00 plus 23% VAT

Applicant Requirements
  • 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)
  • Those who work in regulatory authorities and those in the regulatory sector
Reference No: T2006410-TOP
TOPRA is the professional membership organisation for individuals working in healthcare regulatory affairs.
We work with our members internationally to enable and promote excellence across the healthcare regulatory profession.


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