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Find out when you need to agree a bespoke VAT retail scheme with HMRC.
How to apply VAT rules to supplies, imports and export of gold and investment gold.
Information and guidance on a range of medical devices for users and patients.
How we work with buyers and suppliers to improve the way technology is bought across government and the public sector.
Find out about partial exemption and the methods and calculations to use to see how much input tax you can recover.
Find out about the calculation of the company car benefit charge.
Details of administrative agreements relating to VAT on certain specific transactions between members of trade bodies and HMRC.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to tax a beneficial loan arrangement for a director or employee.
Guidance on Defence and Security Accelerator terms and conditions for funding, contracts and intellectual property rights.
Find out about the requirements and obligations for warehousekeepers of motor and heating fuels in the UK.
Find out about the VAT domestic reverse charge procedure which applies to the buying and selling of certain goods and services.
List of manufacturers and their medical devices granted an exemption by MHRA. The list also includes manufacturers whose exemption expired or was cancelled.
Make sure your technology, infrastructure and systems are accessible and inclusive for all users.
The guide to VAT rules and procedures.
Chargepoint and infrastructure specifications and claim guidance for electric vehicle chargepoint and infrastructure grants.
Supplier declarations are where your UK supplier provides you with information needed to prove the origin of your goods for preferential rates of duty between the UK and other countries.
“A project can’t be delivered by just one person. We need to build strong, flexible, professional and capable teams.” - Nick Smallwood (Head of Project Delivery Function) Project Delivery Function is part of the Civil Service .
Guidance for suppliers and dealers.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
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