3-Hour Virtual Seminar on Human Error Prevention in the Life Sciences

This 3-Hour virtual seminar will explore the true causes and nature of human error, how human error should be investigated, how human error relates to human performance, and the difference between real human error and systems, process, and management deficiencies. It will also address how human error occurs in the planning and execution stages of task performance.

Human Error occurs in all settings. In the world of pharmaceutical manufacturing, the result of that error can result in loss of product or at the most extreme, injury to patients. Human is a frequent occurrance in pharmaceutical manufacturing. It occurs even when every obvious preventive actions have been employed such as effective compliance documentation development and training.

Unfortunately, sometimes these actions are not adequate to prevent these errors from occurring. “Human Error” is sometimes not the cause of issues even though relegated / assigned as the root cause of adverse events with reasons assigned such as “lack of attention to detail” or “failure to follow procedure”. Corrective action in these instances often involve re-training or disciplinary action. These approaches do not seek to understand really why the error(s) occurred.

Learning Objectives:

At the completion of this webinar participants will be able to:

  • Define human error and identify its properties.
  • Explain the cost of human error
  • Explain how human error is manifest in the pharmaceutical setting
  • Explain how potential human error situations are investigated
  • Explain how the real root cause of human error is identified and verified.
  • Define the role of leadership in Human Error reduction
  • Explain and describe the Error Reduction Strategies that are effective in mitigating human
Seminar Agenda:

  • Human error defined
  • Properties of human error
  • When does human error occur
  • Human error and human performance
  • Human error in pharmaceutical manufacturing
  • The role SOPs and Work Instructions play in preventing Human Error
  • Investigating human error
  • Determining and verifying human error root causes
  • The role of leadership in Human Error reduction
  • Human Error Reduction Strategies
  • Human Error Prevention and Reduction Drivers
Who Should Attend:

  • Regulatory Affairs Departments
  • Compliance Departments
  • Quality Departments
  • Manufacturing Departments
  • Production Departments
  • Engineering Departments
  • Operations Departments
  • Research and Development Departments
  • Documentation Departments
  • Laboratory Professionals

FDB3287

Charles Paul

Charles Paul is an instructional designer and management consultant with over 30 years’ experience providing training and consulting services to regulated industries. He has installed quality systems and designed and developed GMP and operational documentation and training programs for foods and beverage, pharmaceuticals, biotech, cosmetics, and consumer product – OTC industries.

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  • Login Information with Password to join the session, 24 hours prior to the webinar
  • Presentation Handout in .pdf format
  • Presentation from the Speaker
  • Feedback form
  • Certificate of Attendance
  • Recording access Information with Password to view the webinar, will be sent 24 hours after the completion of the Live webinar.
  • Presentation Handout in .pdf format
  • Certificate of Attendance
.