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Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Reducing the impact of future pandemics by making diagnostics, therapeutics and vaccines available within 100 days. An independent report on implementation of the 100 Days Mission to G7 Leaders from G7 Chief Scientific Advisers.
A guide to collecting data about your packaging. This is for UK organisations affected by extended producer responsibility (EPR) for packaging.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Reports, guidance and information about improving the quality and quantity of management information within government.
Information on how to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to write up and share your findings
What to do if you think you've spotted a scam pretending to be from Companies House, and examples of scam emails, letters and telephone calls.
Analysis, appraisal, evaluation, modelling and research that has been carried out to inform transport decisions and policies.
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