Course Details

The new UKCA and future UK regulation for Medical Devices and IVDs webinar

Course Area

Medical Devices


Available for 90 days after enrollment

Approximate Course Run Time

1 hour

Continuing Education Units


Course Fee

No charge

E-learning content is available on demand


Course Details


The Medicines and Healthcare products Regulatory Agency (MHRA) has published new guidance on GOV.UK, which sets out how medical devices will be regulated after the transition period with the EU has ended (from 1 January 2021).

Key takeaways and learning objectives

  • The introduction of the new UK route to market and the mark of conformity for devices.
  • The transition period for products already CE marked, following confirmation of recognition of the CE mark until 30 June 2023.
  • The implications of Great Britain not implementing the EU Medical Devices Regulation (MDR) and In Vitro Diagnostics Regulation (IVDR).
  • Outline of how the requirements will impact manufacturers in the UK and EU.

Presenter Information

Join BSI’s Dr Jayanth Katta, Senior Regulatory Lead, to hear the Notified Body perspective on the announcement regarding the new UK Conformity Assessed (UKCA) mark.

Live Online Classes

Certified, convenient, and interactive, with no travel costs.

Private Class

Interested in a private or customized version of this course? Request a quote.


For questions regarding any of our courses, contact us or call 1.800.217.1390.


For questions regarding any of our courses, contact us or call 800.217.1390 (USA) 800.862.6752 (Canada)

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