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How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
This is an explanation of how we process personal data.
Training material and guidance on how to use and implement the International Protocol on the documentation and investigation of sexual violence in conflict.
Provides detailed information on both potential types of information and evidence, and the correct way to process and record such information.
RAIB investigation reports, safety digests, and urgent safety advice by year of publication.
Spreadsheets are a common way to share data. Use this information to help you avoid common errors, improve interoperability and create more accessible spreadsheets.
Sets out key practical issues to consider when planning investigation or documentation.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
The Director may investigate any suspected offence which appears to him on reasonable grounds to involve serious or complex fraud, bribery or corruption.
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