FALLS CHURCH, Va., Feb. 19, 2020 /PRNewswire-PRWeb/ -- How to Deploy Root Cause & CAPA to Minimize Human Error An FDAnews Webinar Wednesday, March 4, 2020, 1:00-2:30 p.m. EST
https://www.fdanews.com/minhumanerror
Do employees fail because of process weaknesses that set them up for failure from the start? Does ones procedures provide necessary information and clearly indicate critical steps, along with warnings or cautions associated with the steps? Does ones systems work for manufacturing or the other way around?
Many variables from procedures, training to workplace environment affect human behavior. One needs to understand human behavior and the psychology of error in order to implement a process dedicated to investigating and fixing human errors.
Human Error Solutions' CEO, an industrial-organizational psychologist and one of the world's few human error reduction experts, Ginette Collazo, Ph.D., is here to explain how to:
Interested in registering multiple sites? Call 888.838.5578 in the U.S. or +1 703.538.7600 globally to learn about our special multisite discount.
Webinar Details: How to Deploy Root Cause & CAPA to Minimize Human Error An FDAnews Webinar Wednesday, March 4, 2020, 1:00-2:30 p.m. EST https://www.fdanews.com/minhumanerror
Tuition: $287 per site
Easy Ways to Register: Online: https://www.fdanews.com/minhumanerror By phone: 888.838.5578 or 703.538.7600
About FDAnews: FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews' print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA's complex and ever-changing regulations
SOURCE FDAnews
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Do employees fail because of process weaknesses that set them up for failure from the start? Does ones procedures provide necessary information and clearly indicate critical steps, along with warnings or cautions associated with the steps? Does ones systems work for manufacturing or the other way around?
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Many variables from procedures, training to workplace environment affect human behavior. One needs to understand human behavior and the psychology of error in order to implement a process dedicated to investigating and fixing human errors.
Human Error Solutions' CEO, an industrial-organizational psychologist and one of the world's few human error reduction experts, Ginette Collazo, Ph.D., is here to explain how to:
- Determine when human error is a causal factor of quality and compliance issues, as established in GMPs
- Gain better control over human error by incorporating human factors in our process, procedures and systems
- Understand the types of human error, including intentional and unintentional errors of omission and commission
- Measure human error rates by using the root cause determination tool and cognitive load tool
- Track human error and determine trends in quality and compliance by root cause coding structure
- Make predictions regarding human error by diagnostic studies and root cause determination tool coding
- Determine CAPA effectiveness by event reoccurrence and root cause recurrence
Interested in registering multiple sites? Call 888.838.5578 in the U.S. or +1 703.538.7600 globally to learn about our special multisite discount.
Webinar Details: How to Deploy Root Cause & CAPA to Minimize Human Error An FDAnews Webinar Wednesday, March 4, 2020, 1:00-2:30 p.m. EST https://www.fdanews.com/minhumanerror
Tuition: $287 per site
Easy Ways to Register: Online: https://www.fdanews.com/minhumanerror By phone: 888.838.5578 or 703.538.7600
About FDAnews: FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews' print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA's complex and ever-changing regulations
SOURCE FDAnews
