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How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Find out about the customs simplified procedure aggregation rules for the Customs Declaration Service (CDS).
Assess your goods, software and technology to determine whether or not they are controlled and require a licence to export.
List of controlled goods that follow the normal import declaration rules if HMRC apply continuity plans due to system issues.
Get a goods movement reference to move goods through locations which use the Goods Vehicle Movement Service.
Project Orbis is a programme to review and approve promising cancer drugs helping patients access treatments faster.
Guidance for EU exporters, exporters from the rest of the world and UK importers, on how to import groupage or mixed load consignments of animal products into Great Britain.
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