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 a licence that lets you import, move and keep normally prohibited material in England and Wales.
These published standards relate to a number of KPIs in the VMD Deliverables and KPI document.
Find out how to move your goods from inward processing into free circulation, another special procedure or re-export.
Find out how to use the digital handshake to get client authorisation for the agent services account.
Use form OS TM03 to terminate the appointment by an overseas company of a person authorised to accept service of documents or a person authorised to represent the company.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
The MHRA is part of the Access Consortium along with the Therapeutic Goods Administration, Health Canada, Health Sciences Authority of Singapore and Swissmedic.
The MHRA will review applications for orphan designation at the time of a marketing authorisation (MA) or variation application.
Formerly part of M18, how to prepare and interpret analytical quality control (AQC) charts to verify the performance of your monitoring method.
The Trade Remedies Authority exists to defend the UK against unfair international trade practices. We investigate whether new trade remedies are needed to prevent injury to UK industries caused by unfair trading practices and make recommendations on appropriate measures to...
Find out how to prove the originating status of your goods and check if you can claim preferential tariff treatment.
The MAA Approvals Division manages and maintains approval schemes covering a range of activities from technical to operational, both on an organisational and individual basis.
Find out how to use the Online Agent Authorisation to get client authorisation for HMRC online services for agents.
How to register an overseas entity and its beneficial owners or managing officers, so it can buy, sell or transfer property or land in the UK.
The way you apply to licence biological products has changed
Submissions related to human medicines need to be submitted directly to the MHRA.
How a marketing authorisation holder should report a defect with a veterinary medicine.
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).