fda medical device training 2017 - Tools for Human Error Reduction -By AtoZ Compliance

Key Take Away:
This root cause analysis training offers practical approaches and tools to address human performance issues in GMP related environments by using a specific methodology to correct, prevent and avoid re-occurrence of these issues.
Overview:
Human error is known to be the major cause of quality and production losses in many industries. Although, it is unlikely that human error will ever be totally 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.
Why Should You Attend:
To work with these challenges it is really important to understand human behavior and the psychology of error as well as understand exactly where the systems weaknesses are, so they can be improved and/or fixed.
Areas Covered In This Webinar:
Background on Human Error Phenomena and measurement.
Importance of Human Error Prevention/reduction.
Quantitative and qualitative information gathering.
Why do we need tools for human error reduction programs?
Training as a tool and human error.
Facts about human error and training.
Human Error as the Root Cause: what to do and how to measure it.
Tools
Prediction
Root Cause Analysis
Cognitive load assessment
Systems available
Human error rate
Floor checklist
Interview questions
Human error rates and other metrics
Trending and tracking
CAPA effectiveness
Metrics and Human Error
KPI’s
Human Error rate
1st time pass rate
Overall equipment effectiveness (OEE)
Trending /Tracking
Learning Objectives:
Understand human error: factors and causes.
Understand the importance: regulatory and business.
Define the process to manage Human Error deviations.
Learn about human error measurement.
Learn about tools for measurement.
Establish Key Performance Indicators.
Define and measure human error rate, cognitive load, and CAPA effectiveness
Identify what I can do to support human reliability.
Who Will Benefit:
Training managers and coordinators
Operations
Manufacturing
Plant engineering
QA/QC staff
Process excellence/improvement professionals
Industrial/process engineers
Compliance officers
Regulatory/legislative affairs professionals
General/corporate counsel
Executive management
For more information, please visit : http://bit.ly/2qUkjE6
Email: support-AT-atozcompliance.com
Toll Free: +1- 844-414-1400
Tel: +1-516-900-5509
Level:
Intermediate
Speakers Profile:
Ginette M. Collazo, Ph.D
Ginette Collazo, PH.D is a human error and human behavior expert. She has spent more than 15 years in technical training, organizational development and human reliability areas.
She has worked with Bristol-Myers Squibb, Johnson & Johnson, Schering-Plough, Wyeth, and has been a consultant with major firms like Abbott, Johnson & Johnson, Perrigo, among many others.
Also has implemented human error reduction programs and technology in many more small and mid-sized drug and device companies.
An active researcher in specialized studies related to human reliability, she is the author of numerous publications on these topics.