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Register to vote Register by 18 June to vote in the General Election on 4 July.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Grievances and disciplinary action at work can be solved by informal discussions, formal procedures, mediation, conciliation or arbitration.
Find the notes for all Declaration Category Data Set tables covered by Appendix 21-25 of the CDS Declaration and Customs Clearance Request Instructions.
Find out what to do when you're moving goods between special procedures in Great Britain and Northern Ireland.
Role, scope, process and how to apply for a review of a procedural decision.
The government response to the review of the operation of sections 6-11 on closed material procedure (CMP) in the Justice and Security Act 2013.
Follow these steps when preparing to make an imports declaration on the Customs Declaration Service.
Find out about the VAT domestic reverse charge procedure which applies to the buying and selling of certain goods and services.
How the MHRA processes variations to Marketing Authorisations (MAs)
The hearing procedure and listed cases before the tribunal.
Guidance for holders of Marketing Authorisations approved in Northern Ireland or the EU/EEA member states who want to bring a product to market in Great Britain.
These published standards relate to a number of KPIs in the VMD Deliverables and KPI document.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
SOPs should take account of regulatory requirements and security practices.
Don’t include personal or financial information like your National Insurance number or credit card details.
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