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How to apply for a traditional herbal registration (THR) to market a herbal medicine in the UK.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
How to use a budget impact analysis to evaluate your digital health product.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
A Randomised Controlled Trial in a Nigerian Tertiary Care Hospital
How traditional herbal medicines and homeopathic medicines will be treated by the MHRA.
A list of herbal medicines currently holding a traditional herbal registration (THR) granted by the Medicines and Healthcare products Regulatory Agency (MHRA).
Information and guidance on a range of medical devices for users and patients.
The regulations about working in any healthcare role, and how to register with the appropriate accredited bodies.
Supporting health and care professionals to improve services by better understanding the health outcomes that some people in the Roma community face.
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 .
Report a problem ('adverse incident') with a medical device or medicine to MHRA using the Yellow Card Scheme
Millions invested in eight innovative companies behind lifesaving new medical technology which could destroy liver cancer tumours, detect Alzheimer’s and quickly spot those at risk of stroke
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
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