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How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
Find out which standards and regulations apply to your product and how to make sure you follow the right procedures.
Use these general provisions to help you determine the origin of your products.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
International trade regulations for materials, equipment, goods and appliances, chemicals and pharmaceuticals, aerospace and defence.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
How product specific rules are used to identify the country of origin when importing or exporting between the UK and EU.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Check what processes are considered as insufficient production under the Trade and Cooperation Agreement.
Rules for moving goods between the UK and EU under the Trade and Cooperation Agreement.
Foresight project looking at the long-term picture for the UK manufacturing sector between now and 2050.
Advice for manufacturers of Class I medical devices for placing products on the UK market
Find out when your Child Benefit payments are due, and payment dates for bank holidays.
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.
For MAHs, manufacturers, wholesalers, retailers (including vets) and feed businesses on the manufacture and movement of veterinary medicines in relation to the NI Protocol and Brexit.
What you need to do to comply with regulations on manufactured goods you place on the EU market.
Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
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