Healthcare 2021 - Preventing Human Error in the Life Sciences

Overview:
This webinar 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.
Why you should Attend: 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 occurrence 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.
Areas Covered in the Session:
What is Human Error?
Nature of human error in pharmaceutical manufacturing
Approaches to investigating Human Error
The root causes that are directly attributable to Human Error
The role of leadership in Human Error reduction
Human Error Reduction Strategies
Human Error Prevention and Reduction Drivers
Who Will Benefit:
Manufacturing
Engineering
Quality
Regulatory functions or Services to include
Machine Operators and Mechanics
Quality Assurance
Technical Services
Laboratory
Regulatory
Engineers
Documentation development and management with titles such as Associates, Technicians, Scientists, Supervisors, Managers, and Directors
Speaker Profile
Charles H. Paul is the President of C. H. Paul Consulting, Inc. - a regulatory, manufacturing, training, and technical documentation consulting firm - celebrating its twentieth year in business in 2017. He has been a regulatory and management consultant and an Instructional Technologist for 30 years and has published numerous white papers on various regulatory and training subjects. The firm works with both domestic and international clients designing solutions for complex training and documentation issues.