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Use these general provisions to help you determine the origin of your products.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Find out what repairs or processing you can do to your goods in a customs warehouse without authorisation, this is known as usual forms of handling.
How to apply for accreditation, comply with your accreditation and packaging waste technical information.
Find out how to validate your facility when you seek approval to open, including special requirements for continuous and blood processors.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
We have more than 10 years’ experience of successfully working with our customers to develop solutions across the radioactive waste lifecycle and provide access to the full range of treatment, logistics, and disposal techniques and technology in the UK, Europe,...
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.
Helping public health practitioners conducting evaluations – using process evaluations to explain how complex interventions work.
Explainer for the pharmaceutical industry on the ongoing implementation of the Veterinary Medicines Regulation relating to applications and authorisations for veterinary medicines.
When HMRC will issue a joint and several liability notice to individuals who have been involved with companies which have become insolvent and have a tax liability with HMRC.
Find out what you can do with your goods when they are being processed or repaired using outward processing.
Find out about customs special procedures and outward processing that allow you to suspend, pay less or pay no duty on goods you import or export.
You can use the bulk import reduced data set to declare one or more low value parcels in a single import declaration when you import goods to Great Britain.
Find out how you can use, process or store similar free circulation goods in place of goods that you have declared for a customs special procedure.
Find out if the goods you're declaring to inward or outward processing are classed as sensitive goods.
Information on how quickly we will process your application.
How to use a quasi-experimental study to evaluate your digital health product.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Check if you should submit a standardised exchange of information using the EU Customs Trader Portal for inward or outward processing.
Don’t include personal or financial information like your National Insurance number or credit card details.
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