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
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
This guidance provides an overview of the different tariffs for products exported to the UK under the DCTS, including how to identify commodity codes.
Information for manufacturers.
The product and service community is for anyone who wants to discuss and learn about managing products and services in government.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How product specific rules are used to identify the country of origin when importing or exporting between the UK and EU.
Use these general provisions to help you determine the origin of your products.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Guidance for healthcare professionals on managing specific medicines and medical devices and using them safely.
How a marketing authorisation holder should report a defect with a veterinary medicine.
Find out which standards and regulations apply to your product and how to make sure you follow the right procedures.
Uses of fluorinated gases (F gases) that are banned or will be banned in the future.
How to display the legal name for your food product.
A collection of guides for anyone working with animal by-products (ABPs), including how to process, transport, store and dispose of them.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
How to use a cost benefit analysis to evaluate your digital health product.
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).