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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
The UK's regulatory framework for strategic export controls and the circumstances where you might need an export licence.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
How the MHRA makes decisions on whether a borderline product is a medical device and which risk class should apply.
To properly classify and manage waste, you must identify when EEE becomes WEEE.
Get help to classify organic chemicals that contain certain permitted additives or can be dissolved in water, for import and export.
Find out about partial exemption and the methods and calculations to use to see how much input tax you can recover.
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