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
Submission dates and how the submissions using the EC decision reliance procedure work.
Decision for applicant Red Bull GmbH against registration number 15278352, applicant successful.
Find UK trade data from HMRC. Look up data about imports, exports, commodities and traders.
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 apply for marketing authorisation via this new procedure.
How to conform with the legal requirements for placing medical devices on the market.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Advice on writing clear notices and maximising replies to your FSNs.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Apply for a higher education course, track your application and accept or reject your offers.
To help you protect, manage and enforce your intellectual property (IP) rights in Laos.
Find registered patents, patent applications and pending patents
How to prepare for implementation and compliance of the Safety Features Regulation.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
To help you protect, manage and enforce your intellectual property (IP) rights in Vietnam.
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
Renew and pay for a GB or European patent online - when renewal is due, fees, renew by post or phone instead
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
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.