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Chris Anderberg, the Quality and Compliance Manager at SCCR, brings over 30 years of experience in research, spanning academic organizations and industry. 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 development. In her presentation, she plans to focus on quality incident reporting, specifically discussing Kappas. The session starts with a brief introduction and addresses initial technical difficulties. Chris expresses her enthusiasm for the topic and sets the stage for the discussion ahead.