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Information to support your recovery after COVID-19.
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
List of Field Safety Notices from 22 to 26 April 2024.
Submission dates and how the submissions using the EC decision reliance procedure work.
How to use a before-and-after study to evaluate your digital health product.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Guidance and support on coronavirus (COVID-19) in Wales.
Browse cases data for specific areas within the UK.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
The official UK government website for data and insights on COVID-19.
How to conform with the legal requirements for placing medical devices on the market.
Advice on writing clear notices and maximising replies to your FSNs.
How to use a case-control study to evaluate your digital health product.
How to do a Getein Biotech rapid nose-only test for COVID-19. Rapid tests show the result on a device that comes with the test.
The epidemiology, symptoms, diagnosis and management of human T-cell lymphotropic virus types 1 and 2 (HTLV-1 and HTLV-2).
Apply for a higher education course, track your application and accept or reject your offers.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
List of fees for consular information in the USA.
A checklist from the Foreign, Commonwealth & Development Office to help British people prepare for travelling and staying safe abroad.
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