Risk Management in Clinical Trials 2015

Topics

• Utilize the basic principles to take a `risk-based approach`
• Risk management methodology
• Prioritise risks and plan mitigation actions where necessary
• Document risks identified

Who should Attend

• Clinical Research Associates
• Data management Teams
• Project Managers
• Monitors
• Academic Research Organizations` Staff
• Statisticians
• Researchers within a healthcare setting
• Representatives of any CROs or other contractors (ePRO etc) who will be supporting clinical trials
• And all clinical research professional embarking on a risk-based approach