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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.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
The way you apply to licence biological products has changed
List of controlled goods that follow the normal import declaration rules if HMRC apply continuity plans due to system issues.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Trade remedies protect domestic industries from unfair practices around imports. The UK’s own independent trade policy includes a trade remedies system.
How product specific rules are used to identify the country of origin when importing or exporting between the UK and EU.
Find out which standards and regulations apply to your product and how to make sure you follow the right procedures.
Check for listed disinfectants for aquaculture; or apply to have your product listed.
Current issues relating to imports and exports of animals and animal products.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
How a marketing authorisation holder should report a defect with a veterinary medicine.
Guidance providing practical information for placing construction products on the Northern Ireland market and unfettered access provisions.
This guidance provides an overview of the different tariffs for products exported to the UK under the DCTS, including how to identify commodity codes.
How to import or move animal by-products from the EU to Great Britain.
Get help to classify electrical equipment such as communication equipment, cameras, and their parts and accessories.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to conform with the legal requirements for placing medical devices on the market.
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