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Common user charge rates and how the charge applies to imports entering Great Britain through the Port of Dover and Eurotunnel.
This page provides information on the outputs and outcomes definitions for the UK Shared Prosperity Fund.
Find out the information you must give to customers on food products and how to give it.
Assessment methods you can use to find the right Digital Outcomes and Specialists supplier for your needs
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
How to assess a planning application when there are protected plants, fungi or lichens on or near a proposed development site.
Find a supplier who can provide a user research studio through the Digital Outcomes and Specialists framework.
Guidance for recruiters on how to set up online pre-employment checking forms using Civil Service Jobs vX.
Accounting for VAT using retail schemes if you're a VAT-registered business and you cannot account for VAT using normal accounting.
Find out how to import your personal belongings, pets and private motor vehicles when moving or returning to the UK.
How GBN’s technology selection process for Small Modular Reactors (SMRs) will work.
If you put EEE on the UK market you must follow rules on both the EEE you sell and the EEE that becomes waste (WEEE).
When you need to apply for consent, how to apply, and the works that you can do without consent.
How the UK supports the use of combined heat and power (CHP) or 'cogeneration', which avoids network losses and reduces emissions.
How to use a micro-randomised trial to evaluate your digital health product.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Guidance to help local councils in developing policies for renewable and low carbon energy and identifies the planning considerations.
Who is eligible to vote in elections and referendums in the UK
How to write requirements for services on the Digital Outcomes and Specialists framework
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
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