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
Covering thalidomide, lenalidomide, and pomalidomide: temporary guidance for pregnancy prevention arrangements for patients taking them during COVID-19
Check the tariff classification for peptide nisin standardised with sodium chloride
Paper and cardboard production can cause significant pollution. This guide describes industry responsibilities for preventing pollution.
The T29 exemption allows you to treat non-hazardous pesticide washings before disposing of them to land.
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Reclaim VAT you've paid on goods and services bought in the UK to use in your business if you’re registered as a business outside the UK.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
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.
The UK Good Laboratory Practice Monitoring Authority (UK GLPMA) recognises that there are potential challenges COVID-19 will present to members of the GLP monitoring programme.
You must register and declare ozone-depleting substances (ODS) for laboratory or analytical uses.
UK Health Security Agency's laboratories provide a comprehensive range of microbiological tests and services.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Permitted critical uses of halons and the deadlines for decommissioning equipment containing halons.
Sets out COVID-19 testing for hospice patients and staff.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
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.