Tag: compliance uk

Certain products can only be sold in the United Kingdom if a UK Approved Body (also known as UK Market Conformity Assessment Bodies) has been involved in the conformity assessment process. Such products include medical devices, PPE, and products belonging to other categories.

In this guide, we explain how you can find UK Approved Bodies, the tasks they carry out, and how much you can expect to pay.  Continue reading UK Approved Bodies: A Complete Guide

UK Approved Bodies are third-party entities that perform steps of conformity assessment procedures according to the requirements of various UK regulations. In this guide, we list several regulations and types of products for which the use of a UK Approved Body is required.

However, note that there may be other regulations and products for which a UK Approved Body is needed.

Continue reading Which Products Require A UK Approved Body?

Electronic products manufactured or imported for sale in the United Kingdom are subject to various labelling requirements. This includes the UKCA mark, and other compliance marks which are inherented from the time the UK was a member of the European Union.

This guide provides an overview of various labelling requirements applicable to electronic and electrical products in the UK.

Continue reading Electronics Labelling Requirements in the United Kingdom

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