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.
The campaign supports the IPO's commitments to raise public understanding, and ultimately respect, for IP rights.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Find out the rules to establish the country of origin of imported and exported goods and to help identify goods which qualify for lower or no Customs Duty.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
How the government monitors imports into the UK.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
What you need to know about and do to comply with the law and keep consumers safe.
Customer declaration of specific uses of the scheduled category 1 or 2 substances (individual transactions).
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Check if you can apply for Authorised Use relief to reduce your payments when you import goods for a specific use. This can include repairs, maintenance or processing.
This guidance explains what rules of origin (RoOs) are and the changes under the Developing Countries Trading Scheme (DCTS).
The government's summary of an amendment to the EU regulation which sets restrictions on the ingredients that can be used in cosmetic products.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Guidance for healthcare professionals on managing specific medicines and medical devices and using them safely.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
OPSS would like to invite any interested parties to submit any scientific information relevant to the safety assessment of cosmetic ingredients.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
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).