Risk Management in Clinical Research 2019

Topics

• Perform Cause-Effect Anaylysis for identified risks and develop mitigation strategy
• Identify and manage risks of clinical trials
• Develop effective Corrective Action Preventive Action (CAPA) Plans
• Review recent noncompliance trends and regulatory focus for Sites, Sponsors, and IRBs

Who should Attend

• Clinical Quality and Compliance Professionals
• Clinical Quality Assurance Auditors
• Project Managers
• Clinical Research Associates
• Regulatory Affairs Professionals
• Medical Monitors
• Clinical Research Coordinators