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 get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Getting a UK background check so you can apply for Global Entry and get through USA border control faster: how to apply, how much it costs
This guidance provides information about permission in principle - a new planning consent route.
If you are developing a site within a coalfield area you may need to give additional consideration to the proposed drainage and infiltration.
Provides guiding principles on how planning can deal with land affected by contamination.
Find out how internet scams work and what to be aware of - misleading websites, report website fraud, suspicious communication and phishing
Documents, certificate, letters, and notes available from the British embassy and consulates in the USA.
How you must control and monitor emissions from your activities that may cause pollution.
Find out how the accessibility monitoring methodology is used to test websites and mobile apps under the Accessibility Regulations
How the Ministry of Defence estate is adapting to climate change, including nature conservation on the estate.
Tell users how accessible your website or mobile app is in your accessibility statement, based on recent testing.
Privacy notice for patients participating in surgical site infection surveillance.
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.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
What animal by-products (ABPs) are, how to set up a site that uses them safely, the paperwork you need, and how to dispose of them.
Pharmacovigilance system requirements
How to work out the VAT on building work and materials if you're a contractor, subcontractor or developer.
Explains planning controls relating to the storage of hazardous substances in England and how to handle development proposals around hazardous establishments.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
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.