Human Error Reduction Model: How to Manage Human Performance Deviations in a Regulated Environment 2016

Key Topics

• Diagnosing your error tolerance, how to get an error reduction program started and how to measure its effectiveness
• How to understand the implications of human error events - how they affect product quality, business operations and regulatory compliance
• Destructive human behavior factors and how to create the effective recommendations to modify them
• How to identify the relationship between CAPA and human reliability and performance expectations
• How to unlock the mystery of root cause analysis and human error
• 5 key elements of an effective human error CAPA system - strategies to address essential system safeguards that must be put in place to prevent and correct problems
• How to assure that improvement is not by chance but by design
• How to understand key obstacles in existing practices - why correctives don`t correct, and preventives don`t prevent
• How to leap past hurdles and predict errors

Who should Attend

Attendees from:

• Process improvement/excellence professionals
• QA/QC directors and managers
• Manufacturing operations directors
• Training directors and managers
• Plant engineering
• Human factors professionals
• Regulatory professionals
• Compliance officers
• Executive management