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 use an interrupted time series to evaluate your digital health product.
The Lambert toolkit is for universities and companies that wish to undertake collaborative research projects with each other.
How to use a crossover randomised controlled trial to evaluate your digital health product.
A guide to documenting how you’ve collected your packaging data, known as your ‘methodology’. Online marketplaces affected by extended producer responsibility (EPR) for packaging must submit a methodology.
How to import animals and animal products to Great Britain (England, Scotland and Wales), the Channel Islands and the Isle of Man from non-EU countries.
Delay paying Capital Gains Tax (CGT) if you transfer your business to a limited company in return for shares, check if you're eligible, let HMRC know if you do not want to claim Incorporation Relief (sometimes called 'business transfer relief')
Learn how to check if your website or mobile app is accessible.
An initiative for companies committed to integrating 10 corporate responsibility principles in their business operations and strategies.
Guidance for manufacturers, importers and distributors.
How to use a quasi-experimental study to evaluate your digital health product.
From 1 October 2024, more materials facilities will need to sample and report their waste. Sampling and reporting will be more detailed and more frequent under the amended regulations.
Find out how to import your personal belongings, pets and private motor vehicles when moving or returning to the UK.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Using an ecological momentary assessment to evaluate your digital health product.
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
How to send information to Companies House through our extensible markup language (XML) schemas, by purchasing software or developing your own.
How to use a behaviour change techniques review 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. 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.