Exam (elaborations)
FDA Adverse Event Reporting - RAC US
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FDA Adverse Event Reporting - RAC US 5 day Report - ANS->803.53 (Device) 5 work days after the day that you become aware that: (a) An MEDICAL DEVICE REPORTING (MDR) reportable event necessitates remedial action to prevent an unreasonable risk of substantial harm to the public health. You m...
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