101 UK Brexit Notes

Connemara Programme October 16 2018 pg. 78 Business: Appointing Nominated Persons Purpose The purpose of this notice is to explain future arrangements for nominated persons (‘authorised representatives’ and ‘responsible persons’) in relation to manufactured goods. These arrangements will apply in the unlikely event that the UK exits the EU without a deal in March 2019. This notice does not cover the following areas:  The role of Qualified Persons and Qualified Persons Responsible for Pharmacovigilance (QPs and QPPVs) for pharmaceuticals. Guidance available here : Batch testing medicines if there’s no Brexit deal a nd Medicines, Medical Devices and Clinical Trials  The role of the Only Representative for chemicals  Authorised Representatives for medical devices For the purposes of this notice, references to EU countries should be read as references to EEA states (Iceland, Liechtenstein and Norway). Before 29 March 2019 Businesses can appoint nominated persons to carry out certain tasks on their behalf. The tasks a nominated person can carry out are defined in different pieces of EU product legislation. Individuals who can carry out the role of nominated person may also be known as authorised representatives and responsible persons. For example, an authorised representative must hold technical documentation about a product and provide this to market surveillance authorities in EU countries upon request. In some cases, they may affix a marking, such as the CE marking, to a product to indicate that the product meets the relevant requirements set out i n legislation . Generally, the appointment of an authorised representative is optional. It is mandatory in the following circumstances:  For some products (such as medical devices and marine equipment) where the manufacturer is not based in an EU country; and  For cosmetics: a responsible person carries out specific duties, including ensuring that the product is safe for human health. Where a business is based in an EU country and placing cosmetics on the EU market, the responsible person is usually the manufacturer itself. After March 2019 if there’s no deal Any UK-based nominated person will no longer be recognised under EU law . This means they will not be recognised as able to carry out tasks on the manufacturer’s behalf. To minimise disruption immediately after exit, existing authorised representatives based in an EU country will continue to be recognised in the UK for a time-limited period. However, new authorised representatives will need to be based in the UK to be recognised under UK law. Examples of EU production regulations that include the role of authorised representatives can be found at Annex A of th e technical notice on ‘New Approach’ product regulation For cosmetics, responsible persons based in an EU country will no longer be recognised by the UK after March 2019 ( Regulation (EC) N° 1223/2009 i s the main EU legislation covering cosmetics and covers the role of the responsible person). Businesses wishing to place cosmetics on the UK market will need to appoint a UK-based responsible person. This is due to specific legal duties assigned to the responsible person and their importance on ensuring the safety of products placed on the market. Implications The implications outlined below relate to UK, EU and third country businesses in the event of the UK leaving the EU in a ‘no deal’ scenario. This notice does not apply to medical devices . A separate notice has been published for medical devices , although some details are subject to forthcoming consultation. Businesses with an existing authorised representative based in an EU country will not be impacted in the short term and can continue to place products on the EU and UK markets in the same way. Businesses with an authorised representative based in the UK will no longer be able to rely on that representative to carry out all the required tasks for products placed on the EU market. Businesses wishing to appoint a new authorised representative to carry out tasks on their behalf in the UK should be aware that the authorised representative must be located in the UK but will be unable to carry out tasks relating to products being placed on the EU market. Businesses placing cosmetic products on the EU market will not be able to use a responsible person located in the UK to place a product on the EU market. Businesses placing cosmetic products on the UK market will not be able to use a responsible person located in an EU country to place a product on the UK market.