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