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Register to vote Register by 18 June to vote in the General Election on 4 July.
Form for a business to register seed marketing operations.
How to account for VAT on services when a vehicle, ship or aircraft is provided, together with a driver or crew for the transport of goods.
Guidance on the European Union regulation on explosives precursors, including licensing, labelling and reporting suspicious activity
These published standards relate to a number of KPIs in the VMD Deliverables and KPI document.
Get authorised to declare goods you bring into Northern Ireland 'not at risk’ of moving to the EU, so that the applicable EU rate of duty will not be payable on those goods.
Find out about a scheme used by individual landlords to avoid paying tax on their property income and reduce Capital Gains Tax and Inheritance Tax.
The New Active Substance Work Sharing Initiative (NASWSI) has successfully approved several medicines through this international collaboration and continues to foster cooperation and strong relationships between its Access partners. The Biosimilar Work Sharing Initiative (BSWSI) builds on this success.
This page includes summaries of the winning bids for the Digital Connectivity Infrastructure Accelerator (DCIA) pilots competition
How to conform with the legal requirements for placing medical devices on the market.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
Information about how to get ESFA funding for post-16 education and training.
How to identify and report harmful trade practices that affect your business when exporting, importing or operating domestically.
Set up and run a business partnership - naming a partnership, registering with HMRC, partnership tax returns and legal responsibilities
The Contract for Difference (CFD) for renewable energy is a key mechanism of Electricity Market Reform.
Marketing authorisations granted in 2023
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
Industry must notify the MHRA if they will not be using these flexibilities
Comply with good pharmacovigilance practice and prepare for an inspection.
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