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
Register to vote Register by 18 June to vote in the General Election on 4 July.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Get endorsement and approval to apply for the Global Talent visa to work in the UK as a leader in arts and culture - architecture, fashion, film, television.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
Standardisation explained.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
Future RAN is an open competition, run by DCMS, that will allocate up to £30 million of R&D funding to projects that support the goals of the government's 5G Supply Chain Diversification Strategy. The competition is aimed at helping to...
Use the case studies to help you decide when your goods may (or may not) go beyond insufficient production.
How to prepare for implementation and compliance of the Safety Features Regulation.
Case study from Armilla.
A list of authorised orphan medicinal products registered by the UK licensing authority.
Applications closed open for the 2018 Nuclear Decommissioning Authority (NDA) Estate Supply Chain Awards on 5 September.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
Guidance for businesses and organisations holding EU trade marks at the end of the transition period.
Guidance for business and government departments.
Anyone in Northern Ireland selling medicines to the public via a website must still comply with the requirement to apply the EU common logo.
Find out about applications to protect traditional terms related to wine products in Great Britain.
Two jewellery businesses with an emphasis on creating bespoke commissions are the joint winners of the HALO Award 2023.
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).