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Reacting to "Human Error" – Moving Beyond "Retraining" As A Response
This Webinar is over| Date | Dec 13, 2016 |
| Time | 01:30 PM EDT |
| Cost | $299.00 |
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Online
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Reacting to "Human Error" – Moving Beyond "Retraining" As A Response
Date: September 27, 2016
Time: 1:00pm-2:30pm, EDT US
Duration: 90 Minutes - Online
Price: $299 - Includes Bonus Handouts!
Course Description:
Regulatory agencies around the world have increased their focus on deviations and root cause analysis, and this process is one of the largest sources of inspectional observations. Frequently identifying “Human Error” as a root cause and “Retraining” as a CAPA is a clear indication to the regulatory authorities that you’re not solving the quality issues and related problems that exist in your organization
In this interactive webinar, we’ll explore a collection of conditions that can contribute to human error – including identifying the ONE condition where retraining may actually help.
Attendees will learn:
Why “Human Error” as a root cause is a red flag – and what to do about it
The ONE time when “retraining” is an appropriate corrective action – and why it isn’t most of the time. Other areas to assess when a situation presents itself as “Human Error’ – to find the true cause of the problem, and generate better CAPAs
How this process applies to our GMP-regulated environments – introduction and links to some research driving what we know about human performance
Who Should Attend
This course will be of benefit to anyone working in a GMP regulated environment on global or domestic scale who is charged with identifying and addressing sources of human error in GMP operations. This includes leadership, management, and other personnel in quality, manufacturing, engineering, and other regulated functions. This course will be of particular interest to those managing, leading and/or working in a training function.
Date: September 27, 2016
Time: 1:00pm-2:30pm, EDT US
Duration: 90 Minutes - Online
Price: $299 - Includes Bonus Handouts!
Course Description:
Regulatory agencies around the world have increased their focus on deviations and root cause analysis, and this process is one of the largest sources of inspectional observations. Frequently identifying “Human Error” as a root cause and “Retraining” as a CAPA is a clear indication to the regulatory authorities that you’re not solving the quality issues and related problems that exist in your organization
In this interactive webinar, we’ll explore a collection of conditions that can contribute to human error – including identifying the ONE condition where retraining may actually help.
Attendees will learn:
Why “Human Error” as a root cause is a red flag – and what to do about it
The ONE time when “retraining” is an appropriate corrective action – and why it isn’t most of the time. Other areas to assess when a situation presents itself as “Human Error’ – to find the true cause of the problem, and generate better CAPAs
How this process applies to our GMP-regulated environments – introduction and links to some research driving what we know about human performance
Who Should Attend
This course will be of benefit to anyone working in a GMP regulated environment on global or domestic scale who is charged with identifying and addressing sources of human error in GMP operations. This includes leadership, management, and other personnel in quality, manufacturing, engineering, and other regulated functions. This course will be of particular interest to those managing, leading and/or working in a training function.
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