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
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
General announcements and latest decisions of the Certification Officer
Look up a trade mark to see if something identical or similar to your brand is already registered.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
Guidance for European Economic Area (EEA)-qualified and Swiss healthcare professionals practising in the UK.
How to use A/B testing to evaluate your digital health product.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Oct - 31 Dec 2023.
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
Check the patents journal to find UK-registered patents granted, published and filed
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
Department of Health and Social Care and MHRA register of electronic export certificates (human).
Information on COVID-19, including guidance on the assessment and management of suspected UK cases.
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.