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
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to apply for marketing authorisation via this new procedure.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
How to apply for a traditional herbal registration (THR) to market a herbal medicine in the UK.
Prescribing or supplying veterinary medicines including requirements for registration and inspection of premises.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
British travellers to the US must register with the Electronic System for Travel Authorisation (ESTA) before their journey
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
Using recommended patterns for workplace wifi networks and sharing infrastructure.
Find out how to declare that your goods have been put to their authorised use, destroyed or re-exported.
Submissions related to human medicines need to be submitted directly to the MHRA.
Information about ensuring blood and blood component safety.
How to obtain an authorisation to wholesale veterinary medicines.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
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. Please fill in this survey (opens in a new tab).