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
Help available and steps you should take if you have a medical emergency or are hospitalised abroad, including for planned treatment.
The Medicines and Healthcare products Regulatory Agency’s (MHRA) Criminal Enforcement Unit (CEU) seized a quantity of suspected unlicensed medical products following coordinated raids at three residential and six business premises in Bolton, Greater Manchester.
The Medicines and Healthcare products Regulatory Agency’s (MHRA) Criminal Enforcement Unit (CEU) seized hundreds of thousands of doses of suspected illegally traded medicines, including powerful prescription-only medicines, following coordinated raids at two residential and two business premises across North Manchester.
How to get fast-track approval of medical devices during COVID-19.
Information about the EU Regulations and their implementation in Northern Ireland
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to apply for repayment of import duty and VAT on protective equipment or medical supplies brought into the UK from non-EU countries from 30 January 2020 up to 31 December 2020.
The government has laid regulations on procurement, patient choice and competition.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
The Medicines and Healthcare products Regulatory Agency (MHRA), working with law enforcement partners, seized more than 15.5 million doses of illegally traded medicines with a street value of more than £30 million during 2023.
How veterinary medicines can be advertised.
How to get state healthcare if you live, work or study in Liechtenstein.
Guidance for veterinary medicines manufacturers and wholesale dealers in GB on selling and supplying products placed on the EU and UK markets before 1 January 2021 and the evidence you may need to provide.
How to use a cost benefit analysis to evaluate your digital health product.
How to get state healthcare if you live, work or study in Belgium.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
This brief provides an overview of the activities that a strategic purchaser should undertake
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
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).