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
The paper tests the effects of plan making on job search and employment
The Pre-Primary O-Class Context in Three Rural Young Lives Communities in Ethiopia
Evidence from Demographic and Health Surveys
Overview of the work of the Letter of Intent (LoI) group (France, Germany, Italy, Spain, Sweden & UK) on the defence industry.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
Guidance you should consider when considering the employee shareholder employment status.
How the MHRA assesses marketing authorisation applications (MAA) for medicines referred under Article 29.
You can make observations on the patentability of a published patent application.
What policy intent is, how to translate it into a user-facing service and collaborate with policy colleagues.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
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 and requires JavaScript).