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Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Sources of advice and financial support for UK farmers exporting agricultural products to the EU and beyond
A checklist for artists, specialists, museum professionals, exhibitors or businesses working or touring in an EU country, Switzerland, Norway, Iceland or Liechtenstein.
VAT treatment of transactions in commodities, commodity derivatives and on terminal markets.
Guidance providing practical information for placing construction products on the Northern Ireland market and unfettered access provisions.
Find out how to apply VAT to charges for postage, delivery services and how to treat direct marketing services involving distribution of printed matter.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Guidance for manufacturers, their authorised representatives and importers.
Guidance for veterinary medicines manufacturers and wholesale dealers in GB on selling and supplying products placed on the EU and UK markets before 1 January 2021 and the evidence you may need to provide.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Find out which supplies of children’s clothing or footwear are zero-rated for VAT.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
Apply for protection against infringements of intellectual property rights on imports into and exports out of the UK.
Submission dates and how the submissions using the EC decision reliance procedure work.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Get authorised to declare goods you bring into Northern Ireland 'not at risk’ of moving to the EU, so that the applicable EU rate of duty will not be payable on those goods.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
This guidance provides an introductory guide to the standards and regulatory requirements that businesses may need to meet, to import and sell goods in the UK.
What packaged goods are, how they are labelled, units of measurements used and compliance with weights and measures regulation.
Guidance for manufacturers, importers and distributors.
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