Our UKCA resources at your fingertips

Download our UKCA webinar faqs to know more about taking devices to market in Great Britain post Brexit.

Hear Dr Jayanth Katta, Head of UK Approved Body, Regulatory Services, talk about BSI's plans as a UK Approved Body and confirm the next steps for Manufacturers to ensure continued access to United Kingdom market from January 2021.

We offer different services for medical device manufacturers, from CE marking under the EU IVDR and MDR, and UKCA marking under the UK MDR 2002, to QMS certification and MDSAP audits.

If you would like further information or want to discuss your next steps, please contact us about your requirements.