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Register to vote Register by 18 June to vote in the General Election on 4 July.
We're inviting views on how future government policy can best achieve the vision set out in the 'Energy retail market strategy for the 2020s', and how the lessons from recent market developments should inform this.
The CMA has outlined 3 key risks to effective competition on AI Foundation Models and has set out plans for further action in the market.
Provides further detail on First Homes and their implementation.
Submission dates and how the submissions using the EC decision reliance procedure work.
Government and Ofgem are conducting a joint review of the current energy retail market design, to ensure that it is fit for the future and puts consumers first.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Find out about cover policy and indicators for countries and territories that are covered by UK Export Finance.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
The way you apply to licence biological products has changed
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
Provides guidance on planning for retail and other town centre uses.
Guidance about compensation to owners and occupiers of business premises once a compulsory purchase order comes into force.
The EU Emissions Trading System Union Registry: how it works, how Kyoto units are used for compliance within the EU ETS and how to participate in carbon allowance auctions.
Remarks by Sarah Cardell, CEO of the CMA, delivered during the 72nd Antitrust Law Spring Meeting. Washington DC, USA.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to renew marketing authorisations for products granted through different routes and at different times.
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