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
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Jan - 31 Mar 2024.
An initiative for companies committed to integrating 10 corporate responsibility principles in their business operations and strategies.
VICH consultation until 15 August 2024 on guidelines relating to the technical requirements for demonstrating pharmaceutical development of veterinary medicinal products.
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
How to apply for marketing authorisation via this new procedure.
Advice to Lisa Osofsky, former Director of the Serious Fraud Office, The Serious Fraud Office, on business appointments after leaving Crown service.
News and guidance on veterinary medicines issues affected by coronavirus (COVID-19).
Use this form to transfer a product licence, also known as a marketing authorisation, to a different owner.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
The CMA is investigating the partnership between Microsoft Corporation (Microsoft) and Mistral AI.
Guidance for the pharmaceutical industry on applying for a marketing authorisation for parallel import (MAPI).
Form L7 for the isolation, identification and toxin detection of clostridium botulinum and Staphylococcus aureus.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
How to apply for simultaneous review of veterinary medicine submissions to the Australian Pesticides and Veterinary Medicines Authority (APVMA) and the VMD.
How to use a contextual inquiry when developing your digital health product.
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.