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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.
Provides detailed information on both potential types of information and evidence, and the correct way to process and record such information.
Training material and guidance on how to use and implement the International Protocol on the documentation and investigation of sexual violence in conflict.
Sets out issues to consider when collecting testimonies or statements from survivors or witnesses.
RAIB investigation reports, safety digests, and urgent safety advice by year of publication.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
Sets out key practical issues to consider when planning investigation or documentation.
Sets out ethical considerations for interviewing and dealing with survivors or witnesses of sexual violence.
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