Training Course B: GCP Inspection Guidance for Clinical Laboratories

This series of 5 training sessions will help attendees understand the compliance requirements concerning the Clinical Trial Directive for running clinical trials and concerning ICH GCP for FDA and EMA compliance. Providing critical assistance to FDA and EMA regulated companies currently carrying out or preparing to conduct clinical trials and helping attendees to understand how to apply project management principles to auditing to ensure efficient and effective quality assurance of drug development.