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

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-reduce-human-error-once-and-for-all-investigations-root-cause-determination-and-capa-effectiveness/

End Date
Start Date
Event Speciality
Venue
For registration/tickets purchase:
https://www.webinarcompliance.com/product/how-to-reduce-human-error-once-and-for-all-investigations-root-cause-determination-and-capa-effectiveness/
Currency Symbol:
$
Event Cost:
200 Onwards
Event Capacity
350
Event Types (Select all that apply)
Medical Conference
Online Medical Event
Event Registration Contact Email
reshmi@webinarcompliance.com
Event Information Contact Email
reshmi@webinarcompliance.com
Notable Speakers
CME Credits
Yes
Abstract Submission Deadline
(+1) 206-575-7771
Medical Events Worldwide
12922 SE 299th Street, Auburn WA 98092 USA