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Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Information and guidance on a range of medical devices for users and patients.
A list of the information required for the operation of the NHS abdominal aortic aneurysm (AAA) screening programme and accompanying guide.
Report a problem ('adverse incident') with a medical device or medicine to MHRA using the Yellow Card Scheme
List of hospitals and medical facilities for British nationals in France
Details of the Yellow Card scheme, which is the system for recording adverse incidents with medicines and medical devices in the UK.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Information on when software applications are considered to be a medical device and how they are regulated.
The Medical Profession brings together doctors from across the Civil Service. Medical Profession is part of the Civil Service .
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