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The National Crime Agency Remuneration Review Body (NCARRB) make independent recommendations to the government on the pay and allowances of National Crime Agency (NCA) officers designated with operational powers. These officers are subject to legislative restrictions on industrial action. The...
Find out what areas the Scottish administration legislates on and how it is structured.
This series brings together all documents relating to legislative supporting guidance on licensing.
This guide explains key elements of EU law and their history. It accompanies the detailed guide 'Review of the balance of competences'.
This announcement outlines the key changes the Architects Act 1997 (Amendment) Regulations 2023 is making to the Architects Act 1997.
Resources for businesses.
Argentina and Kenya are used as case studies to produce evidence for lessons that may apply to other countries
How OPSS contributes to international legal metrology and who to contact.
Who is eligible to vote in elections and referendums in the UK
Rules employers must follow when making staff redundant - consultations, notice periods, compulsory and non-compulsory redundancy and redundancy pay
Guidance for manufacturers, importers and distributors on the Product Security and Telecommunications Infrastructure Act 2022 and Regulations 2023.
This memorandum provides a preliminary assessment of the legislation that underpins the UK’s independent sanctions framework.
This tax information and impact note details changes to the trade remedies legislative regime.
The devolution guidance notes (DGNs) set out advice on working arrangements between the UK government and the devolved administrations.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
A post-legislative scrutiny memorandum covering the Financial Services Act 2012, the Financial Services (Banking Reform) Act 2013, and the Bank of England and Financial Services Act 2016.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
How to apply for marketing authorisation via this new procedure.
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