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:
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.
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 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.