Risk-Based Monitoring and the Quality Risk Management of Clinical Trials 2015

Risk-Based Monitoring and the Quality Risk Management of Clinical Trials 2015 is a conference focused on

• The contribution that Source Data Verification and Review makes to clinical trial safety and quality
• Best approach to drive RBM strategy
• Assess risk and adapt the model to de-risk each study individually
• Change management strategies that have led to effective RBM implementation
• Guide risk mitigation planning by using metrics
• Data integrity
• Improve connectivity between the Site and Sponsor

Who should Attend

• Clinical Research Sites
  • Clinical Research Coordinator
  • Investigator
  • Clinical Research Associate (CRA) or Monitor
  • Site Director
• Pharmaceutical and Medical Device
  • Data Management
  • Clinical Operations
  • Biostatistics
  • Study Monitoring
  • Quality Assurance
• CROs