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 use a quasi-experimental study to evaluate your digital health product.
International trade mark registrations protected in the EU under the Madrid Protocol will no longer enjoy protection in the UK after 1 January 2021.
How to conform with the legal requirements for placing medical devices on the market.
How to object and challenge someone else's trade mark and details of any legal costs involved.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Guidance for businesses and organisations holding EU trade marks at the end of the transition period.
Examples of unacceptable trade marks around protected emblems, internet domain names and your company name.
The European Trade Mark and Design Network has produced a common practice for use when assessing the inherent distinctiveness of figurative trade marks containing descriptive and/or non-distinctive words.
How to use a before-and-after study to evaluate your digital health product.
How GCSEs, AS and A levels are marked and moderated.
When applying to register a trade mark, you must use the classification system to specify the goods and/or services you'll be using it on.
If you use, produce or supply wood packaging material (WPM) to move goods to or from the EU or the rest of the world, you must make sure it meets international standards.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Depending on the objection raised in your examination, you have 2 months to respond through a number of options.
The Contract for Difference (CFD) for renewable energy is a key mechanism of Electricity Market Reform.
Find out about the legal definitions of biofuel products, excise duty rates and the roles and responsibilities of producers from 1 April 2022.
Advice for manufacturers of Class I medical devices for placing products on the UK market
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.