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Chris Anderberg, the Quality and Compliance Manager at SCCR, has over 30 years of experience in research across academic and industry settings. Her expertise encompasses clinical trial management for global studies, GCP compliance audits, regulatory inspections, clinical event education, and the development of policies and procedures. In this session, she will discuss quality incident reporting and delve into the topic of KAPPA. Despite some technical issues, Chris expresses her excitement to share insights on these important subjects.
