Category Archives: UK Post-Deal Published Guidance
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 Living in Ireland Official information for UK nationals moving to and living in Ireland, including guidance on residency, healthcare and driving. Published 14 May 2013 Last updated 31 December 2020 — 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 Get your EU professional qualification recognised in the UK How to get professional qualifications obtained in the EU, Switzerland, Norway, Iceland and Liechtenstein recognised in the UK. Published 31 ...
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 Converting Centrally Authorised Products (CAPs) to UK Marketing Authorisations (MAs), ‘grandfathering’ and managing lifecycle changes This guidance covers ‘grandfathering’ and managing the ...
Guidance Living in Europe Information for UK nationals living in the EU, EEA EFTA, Switzerland and Ireland before 1 January 2021, including guidance on residency and healthcare. Published 30 January 2020 Last updated ...
Guidance Living in Europe Information for UK nationals living in the EU, EEA EFTA, Switzerland and Ireland before 1 January 2021, including guidance on residency and healthcare. Published 30 January 2020 Last updated ...
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 Providing services and setting up a business Steps to take if you want to provide a service or set up a business in the UK. Published 31 December 2020 From: Department for Business, Energy & Industrial ...
Guidance Health professionals and pharmaceutical products (VAT Notice 701/57) How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and ...
Guidance Healthcare for EU citizens living in or moving to the UK Information on accessing healthcare for citizens from EU countries, Norway, Iceland, Liechtenstein and Switzerland living in or moving to the UK. ...
Guidance Visiting the UK as an EU, EEA or Swiss citizen What you need to know about crossing the UK border and visiting the UK. Published 31 December 2020 From: UK Visas and Immigration, Home Office, Department for ...
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 Cross-border civil and commercial legal cases: guidance for legal professionals Published 31 December 2020 Contents 1.Jurisdiction and recognition and enforcement of judgments 2.Special European procedures ...
Foreign travel insurance Wherever you’re travelling, it’s important to take out appropriate travel insurance before you go. Published 22 March 2013 Last updated 31 December 2020 — see all updates From: Foreign, ...
Guidance Healthcare for UK nationals living in Ireland How to get state healthcare if you’re living, working or studying in Ireland. Published 28 August 2019 Last updated 31 December 2020 — see all updates From: ...
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 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 Driving in the EU What UK drivers need to do to drive when visiting the EU Published 31 December 2020 From: Department for Transport, Driver and Vehicle Standards Agency, and Driver and Vehicle Licensing ...
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 ...
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