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You may be able to claim a waiver for goods brought into Northern Ireland so that you do not have to pay duty on those goods.
This A4 document gives information for community groups now the EU Settlement Scheme application deadline (30 June 2021) has passed.
This Statutory Instrument (SI) ensures that key rights and principles in equality law are safeguarded and enshrined in domestic legislation.
How to get state healthcare if you’re living, working or studying in Ireland.
How product specific rules are used to identify the country of origin when importing or exporting between the UK and EU.
This page contains a list of persons and entities to whom financial sanctions have been applied due to their assessed involvement in terrorist activity. This sanctions regime aims to further the prevention of terrorism in th…
Use the online service to report non-customs state aid payments you’ve received to HMRC and view your state aid allowance if you’ve claimed customs duty waivers.
Licence for the export of of dual-use items to EU member states.
This guidance and starter guide has been issued in order to comply with Regulation (EC) 1924/2006 on nutrition and health claims made on foods.
What you need to do to comply with regulations on manufactured goods you place on the EU market.
This guidance clarifies the expectations on the application of the EU guidance on good pharmacovigilance practices (GVP)
How to get state healthcare if you live, work or study in Portugal.
Get a UK Licence for the Community to transport goods by road to or through the EU, Liechtenstein and Switzerland, and the rules you have to follow.
Permits to travel to or through European Conference of Ministers of Transport (ECMT) member countries, and the rules you have to follow.
Guidance on the 150-day assessment timeline for high-quality marketing authorisation applications including information on how to apply.
Belarus is currently subject to UK financial sanctions. This document provides a current list of designated persons.
The process for applicants applying for a Paediatric Investigation Plan (PIP) modification or waiver.
A roadmap outlining the intended timelines for delivering a future regulatory framework for medical devices and an intended policy on international recognition.
There are changes to the legislation of Reference Medicinal Products (RMPs) used to support abridged marketing authorisation applications
What you need to do if you're planning to start higher education in the EU.
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