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Chris Anderberg, the Quality and Compliance Manager at SCCR, has over 30 years of experience in research across academic and industry settings. Her expertise includes clinical trial management, GCP compliance audits, regulatory agency inspections, clinical event education, quality management of clinical trials, and policy development. In the session, she expresses her excitement to discuss quality incident reporting, particularly focusing on KAPPA metrics. Technical difficulties were briefly encountered at the start, but the session is set to delve into critical concepts related to quality management in clinical research.
