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Data, Freedom of Information releases and corporate reports
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
What you need to do before your product can be placed on the Great Britain market with a UKCA mark.
Check the tariff classification for four-wheeled vehicles powered by an electric motor fitted with a hydraulic lifting device and telescopic jib.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
How to use an interrupted time series to evaluate your digital health product.
Information on road traffic devices, such as breath-testing, speed cameras and immobilisation devices.
I-VMS - Frequently asked questions
How the MHRA makes decisions on whether a borderline product is a medical device and which risk class should apply.
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