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Check the tariff classification for a clip-on camera lens attachment made of glass.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Dual citizenship (also known as dual nationality) is allowed in the UK. Read the rules and how to apply.
Check the tariff classification for a heat and moisture exchanging filter.
How to use the dual registration measure if you are a specialist events haulier.
Collection of guidance for companies, partnerships, pension schemes and trusts who may be liable for tax in more than one country and want to avoid paying twice.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Controls on the brokering of goods that could be used as parts or accessories for weapons of mass destruction and need an export licence.
How Union GEA authorisations permit the export of specified controlled dual-use goods from Northern Ireland to certain countries outside the EU.
Check the tariff classification for car wiring kits for motor vehicles.
Assess your goods, software and technology to determine whether or not they are controlled and require a licence to export.
How to use a crossover randomised controlled trial to evaluate your digital health product.
Guide to licensing requirements and restrictions for trade control and the export of controlled military goods, software and technology.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Actions companies need to take to export nuclear-related items.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Check the tariff classification for lace-up low shoes.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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