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.

When
: 12 November 2020
Where: ONLINE
Time: 9:30-17:00 (GMT)


TOPRA is committed to continuing to support the education of regulatory professionals in this unprecedented situation. However, in light of recent developments and the advice from health authorities, we have made the decision for this course to go ahead as an interactive online course on the same date with many opportunities for questions to the speakers. All delegates already booked on the course will be individually contacted and if you require further information please do e-mail meetings@topra.org


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.

Programme

Download the programme for this course here.

Presenters

  • To be confirmed

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

Pricing    

Course fees:
Type Fee
Standard   £360 + 20% VAT* 

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

Those working for regulatory agencies, government agencies or academic institutions 
 
 £270+20%VAT

Those working for charities, patient groups or in full-time education
 £180+20%VAT

*VAT, if applicable, is charged at VAT of 20%

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

Please read the training terms and conditions before booking this course. By booking a place on this course you are agreeing to these terms and conditions.
When
12/11/2020 09:30 - 17:00
Where
ONLINE
Your company name
Your VAT country
Your VAT number
NOTE
Important instructions before booking - If your company name or VAT number does not appear here or you would like to be invoiced using a different VAT number, please email finance@topra.org

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