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Animal by-products (ABPs) you can use to make pet food, how to provide samples, and how to package your products.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Guidance for holders of Marketing Authorisations approved in Northern Ireland or the EU/EEA member states who want to bring a product to market in Great Britain.
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).
Guidance for manufacturers, importers and distributors.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
How to change the ownership from one marketing authorisation (MA) holder to another.
VAT treatment of transactions in commodities, commodity derivatives and on terminal markets.
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.
Information about the EU Regulations and their implementation in Northern Ireland
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Advice for manufacturers of Class I medical devices for placing products on the UK market
Guidance on the planning for mineral extraction in plan making and the application process.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
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