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Chris Anderberg, the Quality and Compliance Manager at SCCR, has over 30 years of experience in research within academic organizations and industry. Her expertise includes clinical trial management for global studies, GCP compliance audits, regulatory inspections, clinical event education, and the quality management of clinical trials, along with policy and procedure development. During the session, she aims to discuss quality incident reporting and related concepts, including kappas, while addressing any technical difficulties encountered.