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Guidance for applicants outside the UK. It explains the steps to applying for and being granted a visa to live in the UK.
Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Information to help you protect, manage and enforce your intellectual property (IP) rights in the European Union and the European Economic Area (EEA).
Information to help you protect, manage and enforce your intellectual property (IP) rights in Brazil.
The following assistance is available to education institutions that hold a Student or Child Student route licence.
Check what you need to do to employ teachers who are non-UK citizens.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
The maritime recovery route map outlines actions that support the maritime sector's recovery from the impacts of COVID-19.
Watch our caseworkers' top tips to make sure your applications are complete and correct. Avoid more than 20 common requisition points.
Information on how to gain a UK CoC for Engineering/Electro-Technical Officers or Engineering Watch Rating Certificate
How investigators and sponsors should manage clinical trials during COVID-19
Funding guidance for early years initial teacher training (EYITT) providers for 2024 to 2025.
Taking the approved driving instructor (ADI) part 2 test - what you need to bring and what happens during the test.
HS2 Ltd advice to government on changes to the Phase 2b route, between Crewe and Manchester and the West Midlands and Leeds.
Get a free permit to join family from the EU, Switzerland, Norway, Iceland or Liechtenstein in the UK - check if you’re eligible, documents you need to apply.
Find out about the progress of improving coastal access – including maps, process and timing – in Kent and London.
Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
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