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Within UL Solutions we provide a broad portfolio of offerings to all the medical device industries. This includes certification, Approved/Notified Body and consultancy services. In order to protect and prevent any conflict of interest, perception of conflict of interest and protection of both our brand and our customers brand, we have processes in place to identify and manage any potential conflicts of interest and maintain impartiality. UL Solutions is unable to provide consultancy services to EU MDD, MDR or IVDD Notified Body, UKCA MD Approved Body or MDSAP Customers.
  • On-demand Webinar

Brexit - New Compliance Regulations - Americas

Gain insights about the new upcoming regulatory changes for UK market access - the UKCA (United Kingdom Conformity Assessed mark - which will come into effect on 1 January, 2021.

Big Ben and Westminster Bridge in the sunset

The transition period after the United Kingdom’s departure from the European Union will end on Dec. 31, 2020. 
The United Kingdom Conformity Assessed (UKCA) Mark will replace the CE Mark on Jan. 1, 2021. 

Key Insights

  • New compliance regulations for UK
  • Placing goods in the EU and UK after the transition
  • Notified Bodies and Approved Bodies changes

Speaker(s)
Gabriella Mazolla, global market access manager, UL
Colin Forrester, business development manager, UL


Webinar date
October 30, 2020
 

Brexit – New Compliance Regulations