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The following guidance has been jointly developed by the Heath Research Authority (HRA) and MHRA, in consultation with the Information Commissioners Office (ICO), on behalf of the UK.
MHRA performance metrics for clinical trials and established medicines assessment.
Sets out COVID-19 testing for hospice patients and staff.
How the supply of medical devices from Great Britain into Northern Ireland works.
How to use an N-of-1 study to evaluate your digital health product.
Tell DVLA you want to surrender your driving licence due to a medical condition.
The pre-clinical evaluation team at VDEC provides a safe and controlled environment to test new vaccines and therapeutics before they progress to clinical trials
Information on clinical trials for medicines, how to apply for authorisation in the UK, how to manage your authorisation, reporting safety issues and details about the MHRA phase I accreditation scheme.
Following this clinical pathway will help immunology services and teams to make sure babies are referred into diagnostic testing in the required timescales.
Use this letter to get evidence of any illness, physical or mental harm caused by domestic violence, if you're applying for legal aid.
Information for applicants in England about the outcome of the National Clinical Impact Awards 2022.
Information about the awards process for applicants, employers, assessors and award holders.
Following MHRA approval of a clinical trial, early breast cancer patients on endocrine-based therapy can benefit from a study with camizestrant.
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
The Advisory Committee on Clinical Excellence Awards (ACCEA) advises health ministers on the presentation of clinical excellence awards to consultants working in the NHS.
How to use a randomised controlled trial to evaluate your digital health product.
Advice for medical professionals to follow when assessing drivers with diabetes mellitus.
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