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Information about changes to the death certification process in England and Wales from 9 September 2024.
Find out what the King's Speech means for you.
Find out about the different types of delivery costs, and which ones you must include or exclude in the customs value if you’re an importer or clearing agent.
This guidance informs stakeholders about upcoming introductions to the Restricted Patient System.
Get consent to introduce (site permit) or remove fish (excluding fish farms): application forms and rules.
Get your goods cleared by the National Clearance Hub when moving goods into, out of, or through the UK.
To protect your design outside of the UK, you usually need to apply in each country you want protection in.
A capitated approach to payment for mental health services with outcomes and risk share.
Guidance for European Economic Area (EEA)-qualified and Swiss healthcare professionals practising in the UK.
Provides an introduction to National Infrastructure Planning Guidance.
Find out what you can do to prevent tree pests and diseases from establishing and spreading.
The Immigration Act will introduce new sanctions on illegal working, prevent illegal migrants accessing services and introduce new measures to enforce immigration laws.
Explaining the background to devolution and how the legislatures and administrations of Scotland, Wales and Northern Ireland work.
Capitation is an example of a potential new payment model to enable integrated care.
An approach to payment for providers of IAPT services that links payment to patient outcomes as well as the provider’s levels of activity.
Find out about partial exemption special methods for government departments.
Check what customs charges apply when using a fast parcel operator to make import and export customs declarations.
Guidance for childcare providers on when you must register with Ofsted or a childminder agency, when you cannot register, and when you do not have to.
How fishing is assessed and managed in marine protected areas (MPA)
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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