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Departments, agencies and public bodies
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Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
A summary of actions related to problems with T34 syringe drivers
What is considered off-label use of a medical device and examples of it.
The EU has published guidance on exemptions for medical devices manufactured and used within EU health institutions, which applies to Northern Ireland-based health institutions, replacing interim guidance from the MHRA.
Dose of nicotine delivered & uptake and consistency of dose.
Guidance for manufacturers who don’t design or manufacture devices but place their names on the product.
This guidance sets out the clinical requirements based on the consensus of what is ‘minimally acceptable’ performance in the opinion of the anaesthesia and intensive care medicine professionals and medical device regulators.
Information for patients who have been prescribed Paxlovid (nirmatrelvir 150mg and ritonavir 100mg) film-coated tablets COVID-19 antiviral medication.
Ten guiding principles that can inform the development of Good Machine Learning Practice (GMLP).
The MHRA has published advice for patients and healthcare professionals
This report reviews data on patient doses and equipment trends in dental X-ray imaging procedures between 2014 and 2017.
Advice on ingredients in nicotine-containing liquids in electronic cigarettes and refill containers.
Advice and guidance on the management and use of point-of-care testing (POCT) in vitro diagnostic (IVD) devices.
UK government interpretation of the requirements for labelling e-liquids for Great Britain
What 'single-use' means and what symbol is used by manufacturers to show this.
General advice on vigilance - electronic cigarettes devices and refill containers.
Information for manufacturers and users of medical devices containing plastic with DEHP phthalates.
Information for patients who have been prescribed Lagevrio (molnupiravir), the COVID-19 oral antiviral medication.
Device-specific guidance for manufacturers on reporting adverse incidents under the vigilance system
Guidance for manufacturers on the regulations that apply to prosthetic, orthotic and ophthalmic devices.
Patient communication about a very low risk to patient safety in response to the field safety notice (FSN) issued by Diffuplast and MHRA.
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