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Chris Anderberg, the Quality and Compliance Manager at SCCR, has over 30 years of research experience in both academic and industry settings. Her expertise includes clinical trial management for global studies, GCP compliance audits, regulatory agency inspections, clinical event education, quality management of clinical trials, and policy/procedure development. After an introduction by Susan, Chris expressed excitement about the session, which will focus on quality incident reporting and include discussions on Kappas. She faced some technical difficulties but managed to resolve them to continue the presentation.