Incidents, Complaints, and Adverse Events (Sterile Compounding)

This SOP establishes the requirements for identifying, documenting, investigating, and responding to incidents, complaints, and adverse events—including immediate documentation on incident or complaint forms, defined reporting timelines, root cause analysis, prescriber and patient notification when appropriate, corrective actions, and review by the quality committee—to ensure patient safety, accountability, and compliance with USP <797>.

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