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so again um as uh i was mentioning um chris anderberg works at sccr as quality and compliance manager um she has over 30 years of research experience working for academic research organizations and industry her knowledge extends to clinical trial management for globe global studies gcp compliance audits regulatory agency inspections clinical event education quality management of clinical trials and policy and procedure development so thank you so much chris for being here with us and i appreciate your time and i hand it over to you you you are muted chris you are muted let me see if i can unmute you there that should be good perfect all right sorry about the technical difficulties ive had these twice this week um thank you very much susan for the very nice introduction im very excited to be here and i wanted to spend our time together talking about quality incident reporting and youll see as we go through were going to be talking about kappas and im hoping that by going through t