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 to ensure the products you make or import comply with the law and are safe for consumers to use.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Approval of a change to the licence of Comirnaty COVID-19 vaccine will enable thawing and re-labelling of the vaccine outside of the NHS
Weights and Measures Act 1985 and subsequent Deregulation Order 1999 (as amended).
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 Approved Documents provide guidance on ways to meet the building regulations.
The MHRA has approved the combined antibiotic cefepime/enmetazobactam (Exblifep 2 g/0.5 g powder for concentrate for solution for infusion)
Information on road traffic devices, such as breath-testing, speed cameras and immobilisation devices.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Registers of authorised manufacturers, wholesale dealer sites and retailers.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Importing investigational medicinal products for use in clinical trials
Find out about the process and costs to apply for Defra disinfectant approval.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Apply to become or identify an approved manufacturer authorised to carry out conformity assessment.
How to register your chargepoints for OZEV chargepoint grant schemes as a manufacturer.
Information to support commercial fishers on under 12 metre English vessels.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
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.