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Chris Anderberg, the Quality and Compliance Manager at SCCR, brings over 30 years of experience in research, including clinical trial management, GCP compliance audits, and regulatory agency inspections. She specializes in clinical event education and quality management of clinical trials, alongside policy development. During the tutorial, she plans to discuss quality incident reporting and kappa statistics. There were some technical difficulties with her audio at the beginning. Chris expresses her excitement for the session and appreciation for the introduction by Susan.
