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The Royal Mint (RM) is the world’s leading export mint, making coins and medals for an average of 60 countries every year. However, its first responsibility is to make and distribute United Kingdom coins as well as to supply blanks...
List of fees for consular information in the USA.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Use this form to notify Companies House of a Single Alternative Inspection Location (SAIL) where company records will be held.
VisitBritain (VB) is the national tourism agency, responsible for marketing Britain worldwide and developing Britain’s visitor economy. It works with UK Trade & Investment as well as airlines, travel operators, global brands and the official tourism bodies for London, England,...
Information about the EU Regulations and their implementation in Northern Ireland
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Reclaim VAT you've paid on goods and services bought in the UK to use in your business if you’re registered as a business outside the UK.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
The UK Good Laboratory Practice Monitoring Authority (UK GLPMA) recognises that there are potential challenges COVID-19 will present to members of the GLP monitoring programme.
Use this form AD03c to tell us which of the company records are held at the single alternative inspection location (SAIL).
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
How to choose data tools and infrastructure that are flexible, scalable, sustainable and secure.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
Find out who can get a free rapid lateral flow test, how to use the test and what your test result means.
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