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Human Error Investigations Root Cause Determination and CAPA Effectiveness - Webinar

  • ID: 4747622
  • Webinar
  • Online Compliance Panel
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This training program will offer attendees an understanding of human error its factors and causes The program will also identify the regulatory and business importance of human error prevention and define the process to manage human error deviations.

Objectives of the Presentation
  • Understand human error: factors and causes
  • Understand the importance: regulatory and business
  • Define the process to manage human error deviations
  • Identify root causes associated with human error deviations
  • Identify what I can do to support human reliability
Why Should you Attend

Human error is known to be the major cause for quality and production losses in many industries. Although it is unlikely that human error will ever be totally eliminated, many human performance problems can be prevented. Human errors start at the design stage. From procedures, training, and workplace environment many variables that affect human behavior can be manipulated reducing the likelihood of these occurrences.

To work with these challenges it is really important to understand human behavior and the psychology of error as well as understand exactly where the systems weaknesses are, so they can be improved and/or fixed. This course will offer practical approaches to address human performance issues in GMP related environments by using a specific methodology to correct, prevent and avoid re-occurrence of these issues.
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  • Dr Ginette M Collazo Dr Ginette M Collazo,


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  • Training managers and coordinators
  • Operations
  • Manufacturing
  • Plant engineering
  • QA/QC staff
  • Process excellence/improvement professionals
  • Industrial/process engineers
  • Compliance officers
  • Regulatory/legislative affairs professionals
  • General/corporate counsel
  • Executive management
Note: Product cover images may vary from those shown
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