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There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How health app content should be reviewed by subject matter experts.
A guide to farming risks, potential problems with public safety and how to avoid accidents
Code of practice on the effective prevention and control of infection by health service providers.
How offender healthcare is managed in prisons and in the community.
Information on COVID-19, including guidance on the assessment and management of suspected UK cases.
How to use a cost effectiveness analysis to evaluate your digital health product.
Proposed legal requirements to provide information about health service products.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Information for healthcare professionals to protect the public from pressure ulcers (bed sores).
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Advice and guidance for healthcare practitioners on the health needs of migrant patients.
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
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