1. Selling in Great Britain (England, Scotland, and Wales):
Since the UK left the EU, the UK government introduced the UKCA mark, which is the primary certification required for most products sold in Great Britain. The UKCA mark indicates that a product complies with UK-specific regulations, which are similar to EU regulations but governed by UK law.
For products sold in Great Britain, the CE mark is no longer mandatory. Instead, manufacturers must ensure their products meet UK requirements, and in many cases, the UKCA mark is necessary. The UKCA mark covers most product categories, including machinery, electrical equipment, personal protective equipment, and medical devices. This mark must be placed on the product, its packaging, or accompanying documentation, and it must comply with the relevant UK regulations.
2. Transition Period for CE Marking:
To give businesses time to adjust to the new UKCA marking system, CE Mark Registration in UK the UK government allowed a transition period for products that were already CE marked before Brexit. For example, products that were CE marked before Brexit could still be sold in Great Britain until January 2023 under the CE mark. After January 2023, however, products sold in Great Britain must bear the UKCA mark, even if they were CE marked previously.
This means that if you plan to sell your product in Great Britain, you will need to switch from CE marking to UKCA marking by the relevant deadline (January 2023). During the transition period, you may continue to use the CE mark for Great Britain, but after the cutoff date, the UKCA mark will be mandatory.
3. Selling in Northern Ireland:
Northern Ireland remains aligned with the EU’s product regulations due to the Northern Ireland Protocol. As a result, the CE mark is still required for products sold in Northern Ireland, even though the UKCA mark is required for Great Britain. Therefore, if you plan to sell your product in Northern Ireland, you must ensure it is CE marked, in compliance with EU regulations, as the UKCA mark does not apply there.
4. Product-Specific Considerations:
Certain types of products, CE Mark Certification process in UK particularly those in regulated sectors like medical devices, pharmaceuticals, and construction products, may have additional considerations. These products may require third-party conformity assessments or certification by a Notified Body in the UK (for UKCA) or the EU (for CE). Additionally, some products may be subject to stricter rules for health, safety, and environmental protection, requiring ongoing compliance with specific regulations.
5. Exporting to the EU:
If you plan to export your product to the EU or the EEA, you will still need to comply with EU regulations and obtain the CE mark, even if the product is intended for the UK market as well. The CE mark is required for products sold within the EU and Northern Ireland, so you will need to obtain CE certification if your product is intended for sale in both the UK and the EU markets.
Conclusion:
In summary, if you are planning to sell your product only in Great Britain after Brexit, the CE mark is no longer required. Instead, you will need to ensure your product complies with UK regulations and affix the UKCA mark. However, if your product is intended for sale in Northern Ireland, it will still require the CE Mark Consulting Services in UK . Additionally, if you are selling in both the UK and the EU, your product will need to meet the appropriate marking requirements for each region. Be sure to comply with the relevant deadlines and regulations to ensure smooth market access in the UK and EU.