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
Register to vote Register by 18 June to vote in the General Election on 4 July.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Check the tariff classification for preparations put up for retail sale.
Use these EU country codes, VAT numbers and foreign language letters to complete an EC Sales List (ESL).
Reported problems with the supply of an animal medicine and the date when the issue is expected to be resolved.
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
Information about new applications, post-licensing, advertising, product information and fees.
Substances that are classed as persistent organic pollutants (POPs) and when you're allowed to use them.
Allocation coefficients and decision
Imposing safeguard measures for imports of certain steel products.
Guidance for industry on flexible approaches we are taking on good distribution practices.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Guidance for veterinary medicines manufacturers and wholesale dealers in GB on selling and supplying products placed on the EU and UK markets before 1 January 2021 and the evidence you may need to provide.
Industry must notify the MHRA if they will not be using these flexibilities
Notices of publication and a consolidated list of references of pre-Exit European Assessment Documents for construction products.
Get help to classify organic chemicals that contain certain permitted additives or can be dissolved in water, for import and export.
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
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).