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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.
Find the notes for all Declaration Category Data Set tables covered by Appendix 21-25 of the CDS Declaration and Customs Clearance Request Instructions.
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.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
This guide sets out who has to apply for a permit, how to apply and explains the other rules covering travel to Antarctica.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Assess your goods, software and technology to determine whether or not they are controlled and require a licence to export.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
This guidance relates to Standard Essential Patents licensing.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
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