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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.
Information for entertainers and musicians, from non-visa national countries, such as EU Member States and the US, visiting the UK for performance and work.
Assess your goods, software and technology to determine whether or not they are controlled and require a licence to export.
Guidance for manufacturers, importers and distributors.
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.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
Export controls on goods that can be used for torture or capital punishment.
Guidance, created in 2012, for those who wish to begin a private prosecution for offences where the Attorney General’s consent is required.
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