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Advice for medical professionals for assessing fitness to drive.
Information about medical devices that the public can buy for personal use and how we make sure they are safe and effective.
Advice for medical professionals to follow when assessing a patient's fitness to drive.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
How to apply for a regulatory advice meeting on medical devices and in vitro diagnostic devices.
A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
What you need to do before your product can be placed on the Great Britain market with a UKCA mark.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Medicines and Healthcare products Regulatory Agency (MHRA) guidance on using medical devices safely.
Advice for manufacturers of Class I medical devices for placing products on the UK market
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