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Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Information on revocation and amendment of an inward processing authorisation.
Information on the types of Transfer of Rights and Obligations.
Information on VAT only inward processing.
Information on what happens if an inward processing authorisation holder does not comply with their conditions for approval.
Information on process and repair.
Advice and guidance on the health needs of migrant patients from Sri Lanka for healthcare practitioners.
Details of how the SSRO supports the MOD and defence contractors.
This is for contracting authorities involved in staff transfers. Its purpose is to help contracting authorities understand the steps that need to be followed.
Guidance for responsible bodies and education settings with confirmed reinforced autoclaved aerated concrete (RAAC) in their buildings.
Environment Agency regulatory position on storing, transporting, bulking up and accepting litter from voluntary litter collections.
Detention services order 1/2018 about the release of detainees on receipt of an IS106 release order or notification of bail granted by a judge of the First-tier Tribunal.
Environment Agency regulatory position on when you can remove airworthy parts from a waste aircraft which is under a care and maintenance programme.
A varying direction which removes expired email addresses from existing patents directions.
What to do if you disagree with the amount of compensation recovered under the compensation recovery scheme after the claim is settled.
A response to the call for input on single-sex spaces guidance launched by the previous government.
Environment Agency regulatory position on when you can store intact shock absorbers and undeployed airbags in otherwise fully depolluted ELVs on hardstanding.
His Majesty’s Passport Office guidance explaining how we return customer’s documents to them when the application is still live.
Advice for manufacturers of DMHTs that qualify as software as a medical device (SaMD) on understanding new post marketing surveillance rules and examples of how they apply.
Information for manufacturers of software as a medical device, detailing events that may cause indirect harm and are therefore reportable.
Mandatory actions and guidance for probation practitioners following the death of a person under supervision in the community.
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