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 show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to use a randomised controlled trial to evaluate your digital health product.
Find out how to value company benefits for your employees.
Information about the aggregate results estimates produced by the Department for International Development.
Government incentives for CHP schemes
How to use a crossover randomised controlled trial to evaluate your digital health product.
This webinar looks at the information an organisation makes available to clients, or potential clients, and how the consumer's expectations can be met.
You do not need to report the result from a COVID-19 rapid lateral flow test in England.
Information and guidance on a range of medical devices for users and patients.
Why it's important to evaluate digital health products that have been developed rapidly and how to choose evaluation methods in these circumstances.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
We publish these summaries when we or the setting need to take action to ensure they are meeting requirements.
Helping public health practitioners conducting evaluations – using economic evaluation to identify the value gained from an intervention.
How to use A/B testing to evaluate your digital health product.
Comply with good pharmacovigilance practice and prepare for an inspection.
Find out about the rules when a benefit is provided as part of optional remuneration arrangements.
The Supply Side Products (SSPs) are unofficial guidance papers on a range of security and justice issues.
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.