Come and discuss the roles and responsibilities of sponsor vs CRO and investigators as they relate to the quality of clinical trials. How can the sponsor monitor an outsourced clinical trial for GCP compliance? We will discuss clinical trial documentation and what happens during a GCP inspection?
Claes Jagensjö, consultant at Jagensjö Pharma Consulting, has 20 years of experience from pharmaceutical companies and Contract Research Organisations in managing national and international Phase I to Phase IV clinical trials.
Please register latest March 26, so we can arrange breakfast for all of us.