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Register to vote Register by 18 June to vote in the General Election on 4 July.
Choose how you’ll make supplementary declarations for goods that you entered into your own records without authorisation.
How to use a crossover randomised controlled trial to evaluate your digital health product.
How to work out the customs value of imported goods that are free of charge, used, rented or leased if you're an importer or clearing agent.
Find out about the different simplified declarations for imports and what you need to do to get authorisation to use them.
Employment Appeal Tribunal Judgment of Mr Justice Kerr on 23 May 2024.
Documents, certificate, letters, and notes available from the British embassy and consulates in the USA.
How to use simplified procedure values to work out the customs value of consignments of whole fruit or vegetables imported into the UK if you're an importer or clearing agent.
How to use the simplified declaration procedure when importing goods into the UK.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Information on cryptosporidium including sources and routes of transmission, symptoms, and general hygiene advice to minimise the spread.
Find out about the transitional guidance on VAT treatment of transactions of specified supplies of finance and insurance services.
How to legally kill your own poultry, cattle, pigs, sheep, goats, rabbits and hares to eat at home.
Find out about exporting products of animal origin (POAO) such as meat, dairy and fish, live animals, plants and plant products.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Find out how the ATA Carnet works, what to do at customs, and what happens if your goods are lost, destroyed or stolen.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
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