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Essentials of European Medical Device Regulatory Affairs

Price

£360

Location

Dublin, Ireland

Date

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?

When:
12 November 2020

Where:
Dublin, Ireland

Cost?

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.

Email info@topra.org

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