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Find out if you’re a trust or company service provider who needs to register for supervision with HMRC under the money laundering regulations.
How to request and use agent assurance codes if you are a UK-regulated agent carrying out verification checks on an overseas entity, and its beneficial owners and managing officers.
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 how to give or view an authority to use deferment, guarantee or cash account to import goods.
Use inward processing to delay or reduce import duties or VAT on goods that you process or repair.
This amended guidance was issued under s 182 of the Licensing Act 2003.
This guidance sets out how the MHRA is handling centralised applications that were still pending on 1 January 2021.
How retained GEA licences authorise the export of certain controlled items to specified countries.
List of manufacturers and their medical devices granted an exemption by MHRA. The list also includes manufacturers whose exemption expired or was cancelled.
The MHRA will review applications for orphan designation at the time of a marketing authorisation (MA) or variation application.
Apply for authorisation of premises for the retail supply of POM-VPS and NFA-VPS veterinary medicines by suitably qualified persons (SQPs).
Apply for Temporary Admission to import goods to the UK, or move goods from Great Britain to Northern Ireland, and use them temporarily before re-exporting them.
How to register an overseas entity and its beneficial owners or managing officers, so it can buy, sell or transfer property or land in the UK.
Guidance on how to prove someone’s identity or give them access to your service or organisation.
Immigration staff guidance on checking whether an asylum applicant's representative is legally authorised to provide advice.
Follow this guidance with help from your CDDO adviser to categorise digital and technology activity in your pipeline.
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
List of authorised organisations for Innovator Founder and Scale-up visas.
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