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
Guidance for European Economic Area (EEA)-qualified and Swiss healthcare professionals practising in the UK.
Recognised bodies, listed bodies, recognised universities, accredited higher learning institutions, bogus degrees
Who and what Ofqual regulates, how to apply to be regulated and what happens when you want to stop being regulated.
Access and unfair practices during recognition and derecognition ballots
Grant support for activities that enhance the quality, quantity, and diversity of tree seed sources in England.
This guidance is on a Union making an application to be recognised for collective bargaining
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Documents, certificate, letters, and notes available from the British embassy and consulates in the USA.
This part of Schedule A1 is about changes to the bargaining unit or where the bargaining unit has ceased to exist
How to assess and report B2C and B2B electrical and electronic equipment (EEE) and waste electrical and electronic equipment (WEEE) products.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
The approach the MHRA intends to take for products approved or pending in decentralised procedure (DCP) or mutual recognition procedures (MRP).
How to use an ethnographic study to evaluate your digital health product.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
How product specific rules are used to identify the country of origin when importing or exporting between the UK and EU.
Methodology used to select places identified for a Levelling Up Partnership in Scotland.
Submissions related to human medicines need to be submitted directly to the MHRA.
Find out how inland pre-clearance checks affect you and what you need to do when we carry out checks on your goods.
What you must do to be a qualifying recognised overseas pension scheme (QROPS) and what you must report.
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. We’ll send you a link to a feedback form. It will take only 2 minutes to fill in. Don’t worry we won’t send you spam or share your email address with anyone.