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Data, Freedom of Information releases and corporate reports
Information on how to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to use an ethnographic study to evaluate your digital health product.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How to write up and share your findings
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
Information about incidents and outbreaks of Ebola and Marburg, both viral haemorrhagic fevers (VHF).
Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
Helping public health practitioners conducting evaluations – using outcome evaluations to find out if an intervention works.
Advice on writing clear notices and maximising replies to your FSNs.
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