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Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
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.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Advice for medical professionals for assessing fitness to drive.
Government outlines action to make UK a world leader in tackling ethnic and other biases in medical devices.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Supporting health and care professionals to improve services by better understanding the health outcomes that some people in the Roma community face.
Advice on writing clear notices and maximising replies to your FSNs.
How investigators and sponsors should manage clinical trials during COVID-19
These terms and conditions set out the requirements of membership of the Secretary of State for Transport’s Honorary Medical Advisory Panels.
Information for patients, healthcare professionals and developers of new medicines
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Information and guidance on a range of medical devices for users and patients.
Information about the EU Regulations and their implementation in Northern Ireland
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