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Chris Anderberg, the Quality and Compliance Manager at SCCR, brings over 30 years of research experience across academic and industry settings. Her expertise encompasses clinical trial management for global studies, GCP compliance audits, regulatory inspections, clinical event education, and quality management in clinical trials, along with policy and procedure development. During the session, she aims to discuss quality incident reporting and introduce the concept of kappas, despite facing technical difficulties at the start. The introduction highlights her appreciation for the opportunity to share her knowledge on the topic.
