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The variability in observed toxicity across studies can be attributed to differences in patient characteristics, treatment regimens, supportive care measures, and study designs [37, 38]

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Related Blog: The Role of GCP in Ensuring Clinical Trial Integrity Importance of Adverse Event Reporting Adverse events (AEs) are unexpected or harmful effects experienced by participants during clinical trials

At US BioTek, we have not issued provocation instructions with our kits or as standard practitioner instructions because this is a clinical decision to be made with an understanding of the above factors