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Black box medicine and transparency Interpretability by design framework PhD Foundation report for the Welcome TrustAuthors Johan Oldish, Hannah Market, Colin Mitchell, and Alison HallAcknowledgements
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Black box medicine refers to medications or medical devices that have a black box warning on their label, indicating that they may be associated with serious or life-threatening risks.
The pharmaceutical company or manufacturer of the medication or medical device is required to file for a black box warning.
The filing process for a black box warning involves submitting relevant safety data to the regulatory authorities.
The purpose of a black box warning is to alert healthcare providers and patients about the potential risks associated with a medication or medical device.
The black box warning must include detailed information about the specific risks and potential side effects of the medication or medical device.
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