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What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Information for British people on medical support in Thailand including mental health, lists of hospitals and care homes and how the British embassy can help.
Information that GPs and other healthcare professionals need to help us provide benefits and welfare services.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Healthcare professionals prescribing montelukast should be alert to the risk of neuropsychiatric reactions in all patients including children and adolescents. Reported neuropsychiatric reactions include sleep disorders, hallucinations, anxiety and depression, as well as changes in behaviour and mood. Healthcare professionals...
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Get a refund of the immigration health surcharge (IHS) if you work in health and care - eligibility, what you’ll get and how to apply.
Only medical professionals can complete this form. A list of eligible medical professionals is in the Details section of this page.
Medical advisory panels work with DVLA to provide expert advice, with the aim of improving road safety. See information on their role and current vacancies.
Information about the EU Regulations and their implementation in Northern Ireland
Information for healthcare professionals to protect the public from pressure ulcers (bed sores).
These terms and conditions set out the requirements of membership of the Secretary of State for Transport’s Honorary Medical Advisory Panels.
Tax and reporting rules for employers providing medical or dental treatment and insurance
Information for patients, public and health care professionals.
Information and guidance on a range of medical devices for users and patients.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
General information for medical professionals about the assessing fitness to drive guide.
List of manufacturers and their medical devices which have been granted an exemption by the MHRA. The list also includes manufacturers whose exemption expired or was cancelled. This information will be listed for 2 months after expiry or cancellation.
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