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How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Assess your goods, software and technology to determine whether or not they are controlled and require a licence to export.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Information about the MHRA regulates medical devices in Northern Ireland and what legislation applies to manufacturers and suppliers.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
Export controls on goods that can be used for torture or capital punishment.
How to export or move fish for human consumption from the UK.
Guidance, created in 2012, for those who wish to begin a private prosecution for offences where the Attorney General’s consent is required.
Find the notes for all Declaration Category Data Set tables covered by Appendix 21-25 of the CDS Declaration and Customs Clearance Request Instructions.
How to apply for a licence to export cultural goods, including antiques, furniture and archaeological items.
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