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
This document contains information about Kuwait to help HM Passport Office staff process passport applications.
Submission dates and how the submissions using the EC decision reliance procedure work.
From 13 May 2024 we are introducing a change to the procedure for new Marketing Authorisation (MA) applications, where a joint assessment of labels is requested.
Employment Appeal Tribunal Judgment of Mrs Justice Eady on 3 May 2024.
The Foreign, Commonwealth & Development Office (FCDO) provides lists of English-speaking lawyers abroad to help British nationals find the legal support they need.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
Blogs where government organisations talk about their work and share information and ideas.
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
How to conform with the legal requirements for placing medical devices on the market.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Check if you need a tuberculosis (TB) test to support your visa application and find an approved clinic in your country
Submissions related to human medicines need to be submitted directly to the MHRA.
Apply for a higher education course, track your application and accept or reject your offers.
How to use a case-control study to evaluate your digital health product.
Guidance for people with symptoms of a respiratory infection including COVID-19, or a positive test result for COVID-19.
Find registered patents, patent applications and pending patents
List of fees for consular information in the USA.
How to use a randomised controlled trial to evaluate your digital health product.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
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.