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Emerging techniques on how to prevent or minimise the environmental impacts of industrial hydrogen production from methane or refinery fuel gas with carbon capture for storage.
How UK organisations that supply or import packaging should comply with extended producer responsibility (EPR) for packaging.
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
Rules for moving goods between the UK and EU under the Trade and Cooperation Agreement.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
This guidance explains what rules of origin (RoOs) are and the changes under the Developing Countries Trading Scheme (DCTS).
Find out about applying for the Spirit Drinks Verification Scheme, how to submit brand information, fees and making sure your production process is compliant.
Find out about the legal definitions of biofuel products, excise duty rates and the roles and responsibilities of producers from 1 April 2022.
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
How to assess household and non-household packaging from 2024 onwards if you’re a UK organisation affected by extended producer responsibility (EPR) for packaging.
Use inward processing to delay or reduce import duties or VAT on goods that you process or repair.
What animal by-products (ABPs) are, how to set up a site that uses them safely, the paperwork you need, and how to dispose of them.
Submit a return (EX606) to declare duty on wine, cider and other fermented products (formally made-wine) each month.
Guidance for manufacturers and distributors of premixtures and feedingstuffs containing veterinary medicines or specified feed additives.
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How a marketing authorisation holder should report a defect with a veterinary medicine.
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