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
How you import from and export to Turkey.
Using metadata to make it easier to catalogue, validate, reuse and share your data.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
Guidance for healthcare professionals on managing specific medicines and medical devices and using them safely.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to submit your periodic safety update report report (PSUR) or periodic benefit risk evaluation report (PBRER)
Information that schools maintained by a local authority must or should publish on their website.
You can use a SIEL to make shipments of specified military or dual-use items to a named consignee and/or end user.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
When you can share information about your case, what you can share and what to do if someone else shares information.
An overview of the work the IPO is undertaking in relation to Standard Essential Patents.
An explanation of how UKHSA processes your personal data when you apply to access it for secondary purposes
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Information that academies – including any educational setting with academy arrangements – and further education (FE) colleges must or should publish on their website.
Find out how and when to make a delayed supplementary declaration if you’re using simplified declarations to bring goods into Great Britain (England, Wales and Scotland).
What the public register is, what details you need to give us, and how the public can access this information.
How to make a request from public bodies and organisations under the Freedom of Information Act (FOIA), how much it costs and how long it takes
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.