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How to import plants, fruit, vegetables, cut flowers, trees, seeds and used agricultural machinery from non-EU countries to Great Britain (England, Scotland and Wales).
How to import plants, fruit, vegetables, cut flowers, trees, seeds and used agricultural machinery to Great Britain (England, Scotland and Wales) from the EU, Liechtenstein and Switzerland.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
Guidance providing practical information for placing construction products on the Northern Ireland market and unfettered access provisions.
Information on OPSS product safety alerts, reports and recalls for unsafe products and resources for consumers, businesses and regulators.
Product security factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Submit a return (EX606) to declare duty on wine, cider and other fermented products (formally made-wine) each month.
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
Our primary purpose is to protect people and places from product-related harm, ensuring consumers and businesses can buy and sell products with confidence. Office for Product Safety and Standards is part of the Department for Business and Trade .
Find out which types of food are zero-rated and which are standard-rated for VAT purposes.
Guidance for suppliers and dealers.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
Uses of fluorinated gases (F gases) that are banned or will be banned in the future.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
A list of upcoming webinars on the UK’s approach to product marking and placing products on the market in Great Britain and Northern Ireland.
Find out the rules to establish the country of origin of imported and exported goods and to help identify goods which qualify for lower or no Customs Duty.
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