CRED IVD Regulatory Affairs for Global Markets

CRED IVD Regulatory Affairs for Global Markets
Increase your impact as a regulatory professional and expand your IVD expertise beyond Europe with this two and a half day course.

When
: POSTPONED 2025
Where: Online



Also available as face to face event, please click here for the face to face registration option

Course overview

This course will look at global markets including the US, Canada, China and Brazil, examining both the regulatory requirements and best  practice for submissions. The course will also cover the latest updates and emerging issues in these key markets and will also focus on wider key areas of Software as a Medical Device and Unique Device Identification.

In the short video below, our training course co-chair Ashleigh Batchen (Regulatory Strategy Principal (UK) at TÜV SÜD), explains how you can benefit by attending this course.

Benefits to delegates

  • Expand your knowledge of the regulatory and best practice requirements for a range of international markets
  • Learn about wider issues impacting multiple markets such as Unique Device Identification
  • Increase your impact as a regulatory professional
  • Meet and learn from experts in the field   
CPD: This course provides 14.5 CPD hours upon successful completion. To learn more about why Continuing Professional Development is important, visit our Lifelong Learning page.

Programme

A tentative course programme is available to download HERE

Presenters

The course will be chaired by Ashleigh Batchen from TÜV SÜD and Stuart Angell from Ivdeologly.

Suitable for

  • Experience regulatory professionals and others such as PRRC's working in IVD regulatory affairs and wanting to expand their knowledge of markets beyond Europe
  • Anyone responsible for regulatory compliance of IVD products
  • Anyone new to IVD regulatory affairs or wanting to get into IVD regulatory affairs who have previously taken the Essentials of IVD Regulatory Affairs course or the European IVD Regulatory Affairs

Pricing  

Standard

  • Member: £850+VAT*
  • Non-member: £1,075+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:
    • Members: £637.50+VAT
    • Non-members:  £806.25+VAT
  • Those working for charities, patient groups or in full-time education:
    • Members: £425+VAT
    • Non-members: £537.50+VAT

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

Terms and conditions

By booking a place on this course you are agreeing to the training terms and conditions

When
19/11/2024 - 20/11/2024
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

Register now