| Define what constitutes an adverse event and review which adverse event warrant reporting |
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| Ensure timely identification and reporting of adverse events associated with Antibody-Drug Conjugates (ADCs) and understand the value of reporting |
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| Describe the purpose of MIDAS and its role in adverse event reporting |
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| Demonstrate how to effectively report adverse events in MIDAS |
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| Review FDA Adverse Event Reporting System (FAERS) for general knowledge and awareness of this vital program |
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