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

  • 29-30 Sep 2016
  • The Westin San Jose, CA, United States

Description

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

Past Events

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

Event Categories

Business: Human Resources (HR), Innovations, Internal Audit & Compliance, Management, Quality assurance
Science: Engineering, Health sciences, Life Sciences & Biology
Technology: Biotechnology

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