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Brexit SOS - A Review of the Challenges and Impact on the Medical Device Industry

Webinar | 1hr 30min | 2:00 - 3:30PM BST

12 June 2019

In the UK medical devices are subject to EU legislation and with Brexit fast approaching the future remains uncertain for manufacturers. Many question marks remain as manufactures wait to see the final outcome of the current withdrawal agreement and future trading relationship between the UK and Europe such as:

  • How will UK notified bodies operate post Brexit?
  • Who will the NBs be?
  • Will the UK adopt the new MDR or stick with the MHRA post Brexit?

This hour and a half long webinar will focus on the latest regulatory updates for the UK and how you can strategize your approach to overcome Brexit uncertainty, finishing with an open Q&A session with peers and our trainer Richard Young. Attendees will have access to the webinar content for an additional month on our Online Academy platform, where you will be able to review the content and use the forum to discuss Brexit with your trainer and peers.

 A recording of the webinar will be made available for those unable to attend the live session and delegates can ask the Trainer questions through a discussion forum.

  • Gain an up-to-date understanding of the on-going revision to the regulatory landscape in the UK
  • Understand how you can best strategise your approach in all eventualities
  • Benefit from first-hand advice provided by our trainer Richard Young, who has had experience managing projects involving Brexit

Regulatory affairs or manufacturing personnel operating in the UK medical device market, from import to export to UK based organisations.  

In addition, this course would benefit those in industry who would like an updated understanding of the full implications of Brexit on the medical device industry.

Richard Young

Richard Young has over 20 years’ experience in the medical device industry with products such as class 3 implants to electromedical infusion systems. Richard has extensive experience in regulatory affairs, GMP (quality), GLP (laboratory testing) and clinical affairs. Richard has held various positions within industry such as QA/RA Manager and Director, Quality Assurance and Regulatory Compliance at various companies including Biomet, Plasma Surgical and Zimmer Limited.