This webinar will explain regulatory background and guidance for sponsor co-monitoring, principles of CRA oversight, tools and methodologies and critical aspects how co-monitoring can improve conduct of your clinical trial. The Trainer will also present real life case studies and examples where either monitoring or site performance had not been adequate and how co-monitoring had helped to resolve these.
Who should attend?
Clinical research and clinical science professionals: including Clinical Research Associates, Project Managers, Project Directors, QA Auditors, Line Managers and anyone with a professional interest in co-monitoring.
Course related: https://www.eccrt.com/courses/sponsor-co-monitoring