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
Register to vote Register by 18 June to vote in the General Election on 4 July.
How to use a randomised controlled trial to evaluate your digital health product.
How to use a multiphase optimisation strategy (MOST) to evaluate your digital health product.
Find out about the SFI actions for integrated pest management, what land is eligible for each action, and what you need to do to get paid.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
Guidance for EU exporters, exporters from rest of the world and UK importers, on how to import groupage or mixed load consignments of animal products into Great Britain (England, Scotland and Wales).
Guidance on the Specific Batch Control (SBC) scheme for release of product on to the UK market.
Find out about gaining approval for a fair partial exemption special method if you deal with partial exemption for insurers.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
How to carry out a risk assessment if you are applying for a bespoke permit that includes discharging hazardous chemicals and elements to surface water.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
Information on how the Department for Education (DfE) and its executive agencies share personal data.
The CMA acts to help NHS patients access combination therapies used to treat serious medical conditions.
How to comply with the exemption from the Veterinary Medicines Regulations that allow certain animal medicines to be sold without a marketing authorisation.
Find out if you will need to use the new UKNI marking and how to use it.
How to apply for authorisation to import, move or keep specified material and the fees you must pay.
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. Please fill in this survey (opens in a new tab).