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
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
How to report details of your disguised remuneration loan scheme and account for your loan charge liability.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Find out about exporting products of animal origin (POAO) such as meat, dairy and fish, live animals, plants and plant products.
Find out what steps you need to take before you calculate how much you can claim for furloughed and flexibly furloughed employees.
How to use an interrupted time series to evaluate your digital health product.
Find out how to import timber and wood material, including the documents, identity checks and plant health inspections required.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How to use a crossover randomised controlled trial to evaluate your digital health product.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Importing investigational medicinal products for use in clinical trials
How to use a cost benefit analysis to evaluate your digital health product.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Advice for medical professionals to follow when assessing drivers with diabetes mellitus.
Pharmacovigilance system requirements
Compare different evaluation approaches and choose an appropriate method.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
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.