Category Archives: Goods – the Single Market
Sub-categories
Common Rules for Imports The general principle products should be freely imported without being subject to any quantitative restrictions (e.g. quotas), unless there are safeguard measures in place. For the purpose of ...
Purpose This notice explains the future arrangements for the regulation of most goods covered by the EU’s New Approach, which includes those regulated under the ‘New Legislative Framework’ as well as machinery. In ...
Purpose This notice provides guidance on how the importing and exporting non-harmonised goods under the mutual recognition principle would be affected in the unlikely event that the UK exits the EU without a deal in ...
NOTICE TO STAKEHOLDERS WITHDRAWAL OF THE UNITED KINGDOM AND EU RULES IN THE FIELD OF CUSTOMS ENFORCEMENT OF INTELLECTUAL PROPERTY RIGHTS The United Kingdom submitted on 29 March 2017 the notification of its intention ...
Brussels, 25 January 2018 NOTICE TO STAKEHOLDERS WITHDRAWAL OF THE UNITED KINGDOM AND EU RULES IN THE FIELD OF IMPORT/EXPORT LICENCES FOR CERTAIN GOODS The United Kingdom submitted on 29 March 2017 the notification ...
Brussels, 23 January 2018 BIOCIDAL PRODUCTS The United Kingdom submitted on 29 March 2017 the notification of its intention to withdraw from the Union pursuant to Article 50 of the Treaty on European Union. This ...
Brussels, 23 January 2018 PLANT PROTECTION PRODUCTS The United Kingdom submitted on 29 March 2017 the notification of its intention to withdraw from the Union pursuant to Article 50 of the Treaty on European Union. ...
22 January 2018 NOTICE TO STAKEHOLDERS INDUSTRIAL PRODUCTS1 The United Kingdom submitted on 29 March 2017 the notification of its intention to withdraw from the Union pursuant to Article 50 of the Treaty on European ...
Brussels, 28 March 2018 NOTICE TO STAKEHOLDERS TYPEAPPROVAL OF CERTAIN VEHICLES AND ENGINES The United Kingdom submitted on 29 March 2017 the notification of its intention to withdraw from the Union pursuant to ...
Guidance Great Britain register on the addition of vitamins and minerals and of certain other substances to foods Published 31 December 2020 Contents 1.Section A: vitamins and minerals that may be added to foods ...
Guidance Supplying investigational medicinal products to Northern Ireland What you need to do to supply investigational medicinal products (IMPs) from Great Britain to Northern Ireland. Published 31 December 2020 ...
Guidance Supplying authorised medicines to Northern Ireland What you need to do to supply authorised medicines from Great Britain to Northern Ireland. Published 31 December 2020 From: Medicines and Healthcare ...
Guidance Regulating medical devices in the UK What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets. Published 31 December 2020 From: Medicines and ...
Guidance Medical devices: UK approved bodies UK approved bodies listed under Medical Devices Regulations 2002 (SI 2002 No 618, as amended) (UK MDR 2002). Published 1 January 2021 Last updated 1 January 2021 — see all ...
Guidance Designated standards Information for businesses. Published 3 December 2020 Last updated 1 January 2021 — see all updates From: Office for Product Safety and Standards and Department for Business, Energy ...
Guidance Orphan medicinal products in Great Britain The MHRA will review applications for orphan designation at the time of a marketing authorisation (MA) or variation application. Published 31 December 2020 From: ...
Guidance Nutrition legislation information sheet Updated 31 December 2020 Contents EU nutrition laws Important information 1.Nutrition Labelling 2.Food supplements 3.Fortified foods / Vitamin and minerals added to ...
Guidance Textile labelling Advice for manufacturers and retailers on textile labelling. Published 31 December 2020 From: Department for Business, Energy & Industrial Strategy Applies to: Wales, England, and ...
Guidance Converting Centrally Authorised Products (CAPs) to UK Marketing Authorisations (MAs), ‘grandfathering’ and managing lifecycle changes This guidance covers ‘grandfathering’ and managing the ...
Guidance Quality and safety of human blood and blood products What blood establishments, blood banks and manufacturers of blood products need to do to ensure the safety and quality of blood and blood products. ...
Guidance Footwear labelling Advice for manufacturers and retailers on footwear labelling. Published 31 December 2020 From: Department for Business, Energy & Industrial Strategy Print this page You must follow ...
Guidance Register to make submissions to the MHRA Submissions related to human medicines need to be submitted directly to the MHRA. Published 31 December 2020 From: Medicines and Healthcare products Regulatory Agency ...
Guidance Placing manufactured goods on the EU market What you need to do to comply with regulations on manufactured goods you place on the EU market. Published 31 December 2020 From: Department for Business, Energy ...
Guidance Using the UKNI marking Find out if you will need to use the new UKNI marking and how to use it. Published 31 December 2020 From: Department for Business, Energy & Industrial Strategy Applies to: Northern ...
Guidance Using the UKCA marking Find out if you need to use the UKCA marking and how to use it. Published 31 December 2020 From: Department for Business, Energy & Industrial Strategy Applies to: Wales, England, ...
Guidance Placing manufactured goods on the market in Northern Ireland What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market. Published 31 December 2020 From: ...
Guidance Registration of clinical trials for investigational medicinal products and publication of summary results This guidance contains information about registration of clinical trials, publishing trial results ...
Guidance Variations to Marketing Authorisations (MAs) How the MHRA processes variations to Marketing Authorisations (MAs) Published 31 December 2020 From: Medicines and Healthcare products Regulatory Agency Contents ...
Guidance Procedural advice for Northern Ireland on applications for European Commission Centralised Marketing Authorisations Processes for marketing authorisations granted before 31 December 2020, or submitted or ...
Guidance Renewing Marketing Authorisations for medicines How to renew marketing authorisations for products granted through different routes and at different times. Published 31 December 2020 From: Medicines and ...
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