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Register to vote Register by 18 June to vote in the General Election on 4 July.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
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.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
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.
The MHRA will review applications for orphan designation at the time of a marketing authorisation (MA) or variation application.
Details of General Licences issued by OFSI
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.
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.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
There are different ways to register depending on which tax service you want to use on behalf of your client.
Submissions related to human medicines need to be submitted directly to the MHRA.
Don’t include personal or financial information like your National Insurance number or credit card details.
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