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. 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).
The webinar will cover:
4. Outline of how the requirements will impact manufacturers in the UK and EU.