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How to work out the customs value for Customs Duty, import VAT and trade statistics if you’re an importer or clearing agent.
Detail on the UK’s position on consultation and cooperation on external security
This glossary of terms has been created to aid leaseholders and residents to understand wording used in the Building Safety Fund guidance and Leaseholder and Resident Service.
Rules and guidance for prisons and staff on conducting external escorts and bedwatches.
How to arrange an effective external review of governance for your school or academy trust, and improve the performance of your board.
This series brings together all documents relating to WO meetings with external organisations
This series brings together all documents relating to Meetings with external organisations
Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
This collection brings together all documents relating to the permanent secretary's meetings with external organisations.
Information to help school leaders plan, develop and implement the new statutory curriculum.
This series brings together all documents relating to DFID ministers' gifts, hospitality travel and meetings with external organisations
Planning the practicalities and managing or conducting your evaluation.
Check the tariff classification for an oval shaped article consisting of crocheted textile fabric.
This guidance is designed to help UKHSA customers and partners to navigate engaging and working with us and to signpost upcoming events and opportunities.
This series brings together all documents relating to HMT senior officials' business expenses, hospitality and meetings with external organisations
The Microsoft 365 Guidance for UK government is a set of recommended configurations for UK government organisations using Microsoft 365
Find the codes which can be used in Data Element 5/23 to identify the location where the goods may be examined for an external temporary storage facility (ETSF) (Appendix 16F).
Submissions related to human medicines need to be submitted directly to the MHRA.
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