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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
The approach the MHRA intends to take for products approved or pending in decentralised procedure (DCP) or mutual recognition procedures (MRP).
Class and permitted use of passenger ships, cargo ships, tankers, tugs, tenders, fishing boats, yachts, commercial vessels, and the required certificates.
Information on trade sanctions, arms embargoes and trade restrictions, including trade controls, transit controls and restrictions on terrorist organisations.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Guidance for claiming annual investment allowance, small pools allowance and writing down allowance for accounting periods that are more or less than a year.
Guidance and information about high consequence infectious diseases and their management in England.
This guidance relates to the legal criteria for determining whether a building is considered a higher-risk building under the Building Safety Act 2022 and the Higher-Risk Buildings (Descriptions and Supplementary Provisions) Regulations 2023. It relates to the definition of higher-risk...
Types of school and how they're run - community schools, academies, free schools, faith schools, state boarding schools.
How to use Method 1 to work out the customs value of your imported goods if you're an importer or clearing agent.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
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.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
The European Union (EU) and European Economic Area (EEA) - which countries are in the EU and EEA, the single market and free movement of goods, capital, services and people
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
A table of rehabilitation periods for the most common sentences and disposals, and example scenarios.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
You can only import certain goods using an ATA Carnet to claim relief under temporary admission in the UK. Some goods have special conditions attached.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
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