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Placing Certain Products On The Northern Ireland Market

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Applicants wishing to place regulated products on the Northern Ireland (NI) markets continue to follow the EU authorisation process. However, regulated products authorised in Great Britain

NEW PRODUCT MARKINGS AND CONFORMITY ASSESSMENT

Northern Ireland Market Report

This guidance is about placing manufactured goods on the market in Great Britain (GB). Great Britain is England, Wales and Scotland. There’s different guidance if you’re: If you placed goods on the market in an EU country (or in the UK) before 1 January 2021, you do not need to do anything. This guidance explains what you need to do for

Placing certain products on the Northern Ireland market For guidance on regulations relating to: food, visit the Food Standards Agency (FSA) Guidance on the regulations as they apply to products being supplied in or into Northern Ireland. December 2024 1. Introduction This Guide is for businesses placing electrical

What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.

Guides on specific product safety and metrology regulations for businesses placing goods on the market in Northern Ireland from 1 January 2021.

Construction Products Regulation in Northern Ireland

  • Placing manufactured goods on the market in Northern Ireland
  • Regulation of medical devices in Northern Ireland
  • UK Conformity Assessment marking comes into effect
  • Placing Goods on GB Market

Information about how the MHRA regulates medical devices in Northern Ireland and what legislation applies to manufacturers and suppliers.

The Office for Product Safety and Standards and the Department of Business, Energy and Industrial Strategy have published guidance on placing certain products on the

Northern Ireland has one foot in the UK door and one foot in the EU door. Find out what is really needed to sell your medical devices in Northern Ireland. EU Regulation 2019/1020 in Northern Ireland Please find below the link for guidance regarding placing goods on the Northern Ireland market after 16th July 2021. Placing certain products on On 1st September, 2020, the Medicines and Healthcare products Regulatory Agency (MHRA) published its latest Guidance outlining the requirements

Guidance providing practical information for placing construction products on the Northern Ireland market and unfettered access provisions.

Article 4 of the EU Regulation on Market Surveillance and Compliance of Products requires that for certain products to be placed on the EU market, there must be an economic Guidance for businesses who place certain products on the Northern Ireland market from 16 July 2021 June 2021

A Northern Ireland business is now considered an importer if they are bringing goods into Northern Ireland from either Great Britain or another non-EEA country and placing

Article 4 of the EU Regulation on Market Surveillance and Compliance of Products requires that for certain products to be placed on the EU market, there must be an economic

This means that certain products on the Northern Ireland market, including medical devices, are required to comply with relevant EU legislation as well as with UK law. For as long as it is in force, Northern Ireland will align with all relevant EU rules relating to the placing on the market of manufactured goods. You must show that your products meet those

Manufacturers must also make certain that procedures are in place to ensure that any products in series production remain in conformity with the relevant product regulations.

While the Northern Ireland Protocol1 (‘the Protocol’) is in force2, Northern Ireland (“NI”) is aligning with relevant EU rules relating to the placing on the market of manufactured goods. PPE If you’re a Northern Ireland business, you’ll still be able to place qualifying Northern Ireland goods on the GB market with an EU conformity assessment marking, such as the CE

The UKNI (United Kingdom Northern Ireland) marking is the new conformity marking for products placed on the market in Northern Ireland but only where a UK based conformity assessment

Also on this site Product compliance when placing certain goods on the Northern Ireland market Check whether you need to use the UKNI marking Placing goods on the market in Northern Ireland You need to use a conformity marking if you are placing certain goods on the This guidance is about placing manufactured goods on the market in Northern Ireland. There’s different guidance if you’re: placing manufactured goods on the EU market

Share this What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market. The government intends to legislate to continue recognition of EU This guide does not cover placing of workplace goods on the marketplace in Northern Ireland or goods from Northern Ireland being placed on the GB market as part of unfettered access. You will be able to place qualifying Northern Ireland goods on the market in Great Britain based on the conformity markings you use in Northern Ireland. For example, as the CE

Using the UKNI marking The Northern Ireland Protocol came into force on 1 January 2021. For as long as it is in force, Northern Ireland will align with all relevant EU rules relating to the placing Guidance on the regulations as they apply to equipment being supplied in or into Northern Ireland. December 2024 1. Introduction This Guide is for businesses placing pressure As laid down in the EU (Withdrawal) Act and the Northern Ireland Protocol, at the end of the Transition Period certain provisions of EU law will be applicable in Northern Ireland (NI). The

Guidance on the regulations as they apply to machinery being supplied in or into Northern Ireland. December 2024 1. Introduction This Guide is for businesses placing Marketplace is a convenient destination on Facebook to discover, buy and sell items with people in your community.