Category: United Kingdom

This article serves as a step-by-step guide explaining how to affix UKCA marking to products manufactured for the UK market. We break down the process into 5 steps from the point of view of a manufacturer managing the UKCA marking process, with additional instructions for importers.

The 5-step UKCA marking process described in this guide can be broadly applied to the following product categories:

• Toys
• Electronics
• Machinery
• Personal Protective Equipment (PPE)
• Medical Devices
• Gas Appliance

Continue reading How to UKCA Mark a Product in 5 Steps

Technical documentation is mandatory for various products sold in the United Kingdom, including toys, electronics, machinery, PPE and medical devices. In this guide, we explain how you can find technical documentation requirements for your products and when you may need to submit it to a third party for review.
Continue reading Technical Documentation Requirements in the UK: A Complete Guide

Creating or obtaining a UK Declaration of Conformity is mandatory when selling most products which require UKCA marking. In this guide, we explain what UK manufacturers and importers must know about creating a DoC, and what the consequences are if you fail to do so.

This article also explains how a UK Declaration of Conformity differs from an EU Declaration of Conformity.
Continue reading Declaration of Conformity Requirements in the UK: A Complete Guide

The UKNI marking indicates that a product has undergone a mandatory third-party conformity assessment performed by a UK approved body. UKNI marking is often affixed together with CE marking to indicate that the assessment has been made by a UK approved body, instead of an EU notified body.

This guide explains what you need to know about the UKNI marking, including when it is necessary, which products you should use it for, and where you should place the marking.
Continue reading What is the UKNI marking?

Despite the UK having left the European Union, certain EU product regulations and directives still apply to goods sold in Northern Ireland. In return, companies in Northern Ireland retain access to the EU single market.

In practice, this means that companies selling products in Northern Ireland may need to ensure compliance with EU requirements and stay up to date with new and updated regulatory requirements.

This guide addresses some common questions concerning the Northern Ireland Protocol, related agreements, and selling products in Northern Ireland.
Continue reading Product Compliance Requirements in Northern Ireland: An Overview

Authorised Representatives are companies established in the United Kingdom appointed by a manufacturer to perform specific duties on the manufacturer’s behalf. Such companies can, for example, communicate with UK authorities.

Some product regulations indicate that it is voluntary for manufacturers to appoint an authorised representative. Other regulations, such as The Medical Devices Regulations 2002, require manufacturers to hire an authorised representative – or “UK responsible person” – if they are established outside the United Kingdom.

Note that the requirements for appointing an authorised representative in Northern Ireland are different because they remain aligned with EU regulations and directives.

This guide answers some common questions concerning authorised representatives, using The Toys (Safety) Regulations 2011 and The Medical Devices Regulations 2002 as the basis.
Continue reading Authorised Representative Requirements in the United Kingdom