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 get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Guidance for prescribing vets on the use of the cascade.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
The actions to take for sourcing medicines in different circumstances.
How to get a marketing authorisation for an Advanced Therapy Medicinal Product (ATMP) so it can be sold and/or supplied in Great Britain.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
How veterinary medicines can be advertised.
There are changes to the legislation of Reference Medicinal Products (RMPs) used to support abridged marketing authorisation applications
How to apply for, update and cancel licences for the manufacture, import and wholesale of human and veterinary medicines.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
The MHRA is undertaking a public consultation on proposals to end the 'sell through' of unlicensed herbal remedies legally on market at April 2011.
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.