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Chris Anderberg, the Quality and Compliance Manager at SCCR, has over 30 years of research experience in academic and industry settings. Her expertise includes clinical trial management for global studies, GCP compliance audits, regulatory inspections, clinical event education, quality management of clinical trials, and policy development. In her presentation, she aims to discuss quality incident reporting and will cover topics related to Kappas. The session begins with a technical issue regarding her microphone, which is quickly resolved, allowing her to express her gratitude for the introduction and her enthusiasm for the discussion ahead.