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Register to vote Register by 18 June to vote in the General Election on 4 July.
Information and guidance on a range of medical devices for users and patients.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Providing vital research into COVID-19 immunity and vaccine effectiveness nationally.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Advice for manufacturers of Class I medical devices for placing products on the UK market
Lists of English-speaking doctors, medical facilities and practitioners around the world to help British people abroad access healthcare.
How to use a patient-reported outcomes and experiences study to evaluate your digital health product.
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.
A new call for evidence launched today aims to capture and consider views about how the duty of candour is honoured, monitored and enforced.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Foreign, Commonwealth & Development Office (FCDO) advice for lesbian, gay, bisexual and transgender (LGBT+) people travelling abroad.
Information about the EU Regulations and their implementation in Northern Ireland
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
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