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Find out how to prove the originating status of your goods and check if you can claim preferential tariff treatment.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Find out which radioactive sources you need a licence to export and how to apply for one.
How to write clear and effective field safety notices (FSNs) for medical devices.
Find out what information you need to send HMRC before you make a claim for R&D Corporation Tax relief.
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