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Guidance on the management of the public health risks from fish pedicures.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
Zambon SpA is recalling an affected batch as a precautionary measure due to out of specification results for unknown impurities during ongoing stability testing.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
List of Field Safety Notices from 2 to 6 June 2025.
Tax and reporting rules for employers providing medical or dental treatment and insurance.
Check the tariff classification for Swim Spas.
Information about medical devices that the public can buy for personal use and how we make sure they are safe and effective.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
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