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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.
The approach the MHRA intends to take for products approved or pending in decentralised procedure (DCP) or mutual recognition procedures (MRP).
Use this form to apply to register one or more designs for which registration has been deferred.
Get help to classify electrical equipment such as communication equipment, cameras, and their parts and accessories.
Find out about group and divisional VAT registration and the forms you should use to apply.
Find out which plastic packaging components are exempt or excluded from the tax, and if the packaging counts towards the 10-tonne threshold for registration.
The CMA has accepted commitments offered by Google that address the CMA’s competition concerns resulting from investigating Google’s proposals to remove third-party cookies and other functionalities from its Chrome browser.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Find out which motor vehicles you can and cannot claim a payment for using the scheme.
Find out which locations you need to submit an ‘arrived’ export declaration at before moving goods and where to take the goods if they need to be checked.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Find out what records and invoices you need to keep as part of the second-hand motor vehicle payment scheme.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
How to use a randomised controlled trial to evaluate your digital health product.
How to use Method 1 to work out the customs value of your imported goods if you're an importer or clearing agent.
International trade mark registrations protected in the EU under the Madrid Protocol will no longer enjoy protection in the UK after 1 January 2021.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Find out the locations where you need to submit an import declaration before your goods depart for Great Britain (England, Scotland and Wales).
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
The prohibitions and restrictions on the import of animal furs and skins into the UK and the export of salmon and trout.
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