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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.
  • Guide

Preparing for UKCA Compliance eBook: An Introduction to Marking Needs for Access to the U.K. and EU Markets

This guide explains how UL Solutions can help manufacturers transition from the CE to UKCA marking, and maintain both markings for broader market access.

Port, containers, Ship, plane distributing products for market access

Businesses must prepare for the end of CE marking recognition on products sold or distributed in the U.K.

Although the EU will continue to require CE marking for products with harmonized European standards, England, Scotland and Wales will require the new U.K. Conformity Assessment (UKCA) marking.

In order for building products and materials manufacturers to avoid supply chain complications, ensure proper vendor arrangements and mitigate delays after UKCA marking is enforced, is to: Understand common pitfalls, make necessary preparations and find an Approved Body partner who can help achieve market access.

This guide explains:

  • Similarities between CE and UKCA markings.  
  • Common pitfalls when pursuing UKCA compliance. 
  • Actions to consider as you prepare for the UKCA marking.
Download our guide
Preparing

Preparing for UKCA Compliance: An introduction to marking needs for access to the U.K. and EU markets

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