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Register to vote Register by 18 June to vote in the General Election on 4 July.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
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.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Guidance on managing and using bed rails safely.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
List of Field Safety Notices from15 to 19 April 2024.
Information and guidance on a range of medical devices for users and patients.
Extending the period of exemption from the Anti-Dumping Duty on open mesh fabrics of glass fibres, for certain Indian producers.
Find out when it's possible to get zero-rated supplies on medical and research goods and services that have been funded by charities.
Guidance on decontamination and infection control, including surgical instruments, dental equipment, endoscopes and benchtop steam sterilizers.
How to get fast-track approval of medical devices during COVID-19.
Advice for manufacturers of Class I medical devices for placing products on the UK market
List of Field Safety Notices from 20 to 24 May 2024.
The MSA is a unit of the Defence Logistics Organisation responsible for the provision of medical, dental and veterinary supplies to the Armed Forces.
Following MHRA approval of a clinical trial, early breast cancer patients on endocrine-based therapy can benefit from a study with camizestrant.
Hospitals register to use the surgical site infection surveillance service (SSISS) to track infections and patient outcomes.
List of Field Safety Notices from 16 to 20 October 2023.
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