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How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Add metadata to data you are publishing so search engines can find the data you’ve published and display structured results for users.
How to use a quasi-experimental study to evaluate your digital health product.
This guidance supports IT staff who manage the school's ICT network in preparation for check administration.
Use these general provisions to help you determine the origin of your products.
Information and guidance about the multiplication tables check.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
Find out about the customs simplified procedure aggregation rules for the Customs Declaration Service (CDS).
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