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Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Find out how to prove the originating status of your goods and check if you can claim preferential tariff treatment.
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Pharmacovigilance system requirements
Information on how to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
This guidance relates to Standard Essential Patents licensing.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
The EU Emissions Trading System Union Registry: how it works, how Kyoto units are used for compliance within the EU ETS and how to participate in carbon allowance auctions.
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