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Register to vote Register by 18 June to vote in the General Election on 4 July.
Submission of notifications for northern Ireland under article 20 of directive 2014/40/EU.
This tax information and impact note outlines a new power to make regulations to to make regulations to make temporary modifications to the Income Tax (Earnings and Pensions) Act 2003 in the event of a disaster or emergency of national...
The CMA has accepted commitments offered by Google that address the CMA’s competition concerns resulting from investigating Google’s proposals to remove third-party cookies and other functionalities from its Chrome browser.
Check the tariff classification for agarose beads chemically modified with 10% by weight of protein A.
How to market, trial and release GMOs.
The fishing industry is being reminded that changes to some types of vessels must be signed off for safety reasons because of the serious risk they will become unstable as a result.
Options for amending proposals that have planning permission.
The CMA has issued a new decision and order, following the Court of Appeal judgment and order. The CMA’s decision is in respect of the appeal brought by SSE against Ofgem’s decisions to accept code modifications on charges to generators...
Form REMO 8: Application to obtain or have modified a decision in matters relating to maintenance obligations.
Decision letters by the Secretary of State for Levelling Up, Housing and Communities which modify Article 4 directions.
A guide on Armed Forces Pensions and how they may be affected by National Insurance Modification.
Covering thalidomide, lenalidomide, and pomalidomide: temporary guidance for pregnancy prevention arrangements for patients taking them during COVID-19
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
Applications to vary or revoke a modification or condition, or to change the terms of a Section 38 consent.
RA Withdrawn – Content duplicated in RA 5303, RA 5304 and RA 5615.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
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