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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 notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Guidance on Defence and Security Accelerator terms and conditions for funding, contracts and intellectual property rights.
Submit your research to Athena; Dstl's central repository of MOD-sponsored scientific and technical research reports.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
A to Z on content relating to infectious diseases.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
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