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How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Find out which radioactive sources you need a licence to export and how to apply for one.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
The following guidance has been jointly developed by the Heath Research Authority (HRA) and MHRA, in consultation with the Information Commissioners Office (ICO), on behalf of the UK.
Guidance for those conducting research and development on genetic resources.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
This guidance relates to Standard Essential Patents licensing.
Guidance for Applicants wishing to apply for a Promising Innovative Medicines designation, pre-submission meeting or an EAMS Scientific Opinion.
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