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Check what processes are considered as insufficient production under the Trade and Cooperation Agreement.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
Check when packaging is classified as a finished plastic packaging component, and what is meant by substantial modifications, to find out if you must register for the tax.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
When a material is waste, is a by-product or meets ‘end of waste’ status.
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.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
Use the case studies to help you decide when your goods may (or may not) go beyond insufficient production.
What you need to know about and do to comply with the law and keep consumers safe.
Use these general provisions to help you determine the origin of your products.
Use inward processing to delay or reduce import duties or VAT on goods that you process or repair.
Requirements for Biological Veterinary Medicinal Products other than Immunological Veterinary Medicinal Products.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
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.
Licence and registration application information for companies that deal in precursor chemicals.
Get help to classify various items of iron and steel, primarily those classified under chapter 72.
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