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Chris Anderberg, Quality and Compliance Manager at SCCR, has over 30 years of research experience in academic and industry settings. Her expertise includes clinical trial management, GCP compliance audits, regulatory inspections, clinical event education, quality management of clinical trials, and policy development. In the tutorial, Chris expresses excitement about discussing quality incident reporting, specifically focusing on KAPPAs, and aims to cover key concepts in the session. She acknowledges a few technical difficulties at the start and thanks Susan for the introduction.