We use some essential cookies to make this website work.
We’d like to set additional cookies to understand how you use GOV.UK, remember your settings and improve government services.
We also use cookies set by other sites to help us deliver content from their services.
You have accepted additional cookies. You can change your cookie settings at any time.
You have rejected additional cookies. You can change your cookie settings at any time.
Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
OIM report suggests trade between UK nations is not a challenge for most, while policy design can minimise disruption.
Submission dates and how the submissions using the EC decision reliance procedure work.
Provides further detail on First Homes and their implementation.
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.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Find out about cover policy and indicators for countries and territories that are covered by UK Export Finance.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
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.
Find out which stocks and shares you can purchase, make or hold in an investor's stocks and shares ISA.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Provides guidance on planning for retail and other town centre uses.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
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.
How to renew marketing authorisations for products granted through different routes and at different times.
The way you apply to licence biological products has changed
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.
Don’t include personal or financial information like your National Insurance number or credit card details.
To help us improve GOV.UK, we’d like to know more about your visit today. Please fill in this survey (opens in a new tab).