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Form PH7: Application by site owner for a determination that the owner may require an occupier to re-site the occupier's home temporarily to another pitch on the protected site.
Guidance on activities that may require a marine licence.
Documents, certificate, letters, and notes available from the British embassy and consulates in the USA.
Fill in this RMOP form to get approval from APHA to transport pets or assistance dogs to England, Scotland or Wales.
Use form BSA3 to apply for an order determining whether a landlord failed to provide information or documents, and to require they are provided.
Advice for state-funded school admission authorities, independent schools, local authorities and parents.
This note is part of the statutory guidance under s215 of the HRA 2008 (from 1 April 2024)
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
The UK's regulatory framework for strategic export controls and the circumstances where you might need an export licence.
The process for applicants applying for a Paediatric Investigation Plan (PIP) modification or waiver.
Who is eligible to vote in elections and referendums in the UK
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Find out how to export live fish, molluscs and crustaceans for farming, ornamental, or any other purpose except direct human consumption
Explains planning controls relating to the storage of hazardous substances in England and how to handle development proposals around hazardous establishments.
Export controls on goods that can be used for torture or capital punishment.
SLC is growing its understanding of vulnerability and additional support needs with the introduction of the new initiative.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
What we require from each different type of landlord and the approach we will take
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