Human Error 2022 - How To Reduce Human Error Once And For All – Investigations, Root Cause Determination and CAPA Effectiveness

How To Reduce Human Error Once And For All – Investigations, Root Cause Determination and CAPA Effectiveness
Product Id : XF3210
Category : Cross Functional, Food, Drugs & Biologics, Medical Devices, Quality
Presenter : Dr. Ginette Collazo
Scheduled On : March 10 2022 1:00 pm
US/Canada (Eastern Time - ET)
Duration : 90 Minutes
Human error is known to be the primary cause of quality and production losses in many industries. Although it is unlikely that human error will ever be 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 essential to understand human behavior and the psychology of error as well as understand exactly where the weaknesses of the system are so that they can be improved and/or fixed.
This course offers practical approaches and models to address human performance issues in GMP related environments by using a particular methodology to correct, prevent and avoid reoccurrence of these matters.
Why You Should Attend:
This training would provide tools that can be implemented and used after this event. These include practical tools. We will discuss human error categories, near root causes and root causes for these events. We will discuss latest trends in human error issues in the industry.
Learning Objectives:
Error Reduction System
HES Tools
Cognitive load tool
Definition of Human Factors Categories (HFC)
Importance of each HFC
Learn the Human Error Risk Multipliers
Recommendations for each HFC
Implementing the program
Metrics and KPI’s
Areas Covered in the Session :
Human Error as the Root Cause
What is Human Error
How is Human Error controlled?
Root Cause Determination
6 step method for error prevention
Human error rates and measurement
Trending and tracking
Prediction
CAPA effectiveness
Who Should Attend:
Quality Assurance Departments
Quality Control Departments
Training Managers and Coordinators
Research and Development Departments
Regulatory Affairs Departments
Manufacturing Departments
Engineering Departments
Operations Departments
Production Departments
Compliance Departments
Plant Engineers
Process Excellence / Improvement Professionals
Industrial / Process Engineers
Please click on the following link to Register :
https://www.webinarcompliance.com/product/how-to-r...