Data Integrity in Clinical Trials 2018

Topics

• Potential impact of compromised data integrity
• Principles of Research Data Integrity
• QA supports for data integrity and quality
• Detecting issues with clinical data quality and integrity

Who should Attend

• Clinical Monitors, Study Nurses and Investigators
• Employees involved in Designing, Conducting, Evaluating, and Documenting of Clinical Trials
• QA Managers, Project Managers
• Validation Managers
• Pharmaceutical Companies, Sponsors, Contractors (for example CROs, analytical labs) and Vendors for Electronic Systems (including hosting partner)
• Data Managers and Statisticians
• Inspectors Responsible for Performing GCP Inspections and Needing to understand and Assess Data Integrity