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
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
How a marketing authorisation holder should report a defect with a veterinary medicine.
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
We are producing guidance and information for industry, healthcare professionals and patients covering the coronavirus (COVID-19) outbreak.
Trade remedies protect domestic industries from unfair practices around imports. The UK’s own independent trade policy includes a trade remedies system.
Find out which regulations apply to your products and where to go for further information on how to comply with them.
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
The way you apply to licence biological products has changed
Add your product to the Energy Technology List - the list of energy saving products eligible for Enhanced Capital Allowance tax relief
Guidance on defining intended purpose for Software as a Medical Device (SaMD), to help SaMD manufacturers in meeting their statutory obligations.
Notices of publication and a consolidated list of references of pre-Exit European Assessment Documents for construction products.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
How to begin with evaluating a digital health product, including when to evaluate, budgeting and getting support.
The Open Networks Research and Development (R&D) Fund is the £250 million government supported programme to deliver upon the UK’s 5G Supply Chain Diversification Strategy.
Find out about applying for the Spirit Drinks Verification Scheme, how to submit brand information, fees and making sure your production process is compliant.
Find out how you can use, process or store similar free circulation goods in place of goods that you have declared for a customs special procedure.
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.