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Chris Anderberg, 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, Good Clinical Practice (GCP) compliance audits, regulatory agency inspections, clinical event education, and the quality management of clinical trials, as well as policy and procedure development. In a recent session, she expressed her enthusiasm for discussing quality incident reporting and the importance of KAPPA analyses. The session faced some technical difficulties at the start but Chris was eager to share her insights.
