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
Past Events
Human Error Reduction Model: How to Manage Human Performance Deviations in a Regulated Environment 2016 - 29-30 Sep 2016, The Westin San Jose, California, United States (61387)
Important
Please, check "Human Error Reduction Model: How to Manage Human Performance Deviations in a Regulated Environment" official website for possible changes, before making any traveling arrangements