Sign for Notice Everyday    Sign Up| Sign In| Link|

Our Sponsors

  • ESTA - Electronic System for Travel Authorization
Receive Latest News

Share Us

Controlling human error in the manufacturing floor

View: 131

Website | Edit Freely


Deadline: May 11, 2017 | Date: May 11, 2017

Venue/Country: Online

Updated: 2017-03-10 14:54:00 (GMT+9)

Call For Papers - CFP

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. 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. This course offers practical approaches and models to address human performance issues in GMP related environments by using a specific methodology to correct, prevent and avoid re-occurrence of these issues.

Why Should You Attend

This training would provide tools that can be implemented and used after this event. This includes 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.

Areas Covered in this Webinar

Background on Human Error Phenomena

Importance of Human Error Prevention/reduction

Training and human error

Facts about human error

Human Error as the Root Cause

What is Human Error

How is Human Error controlled?

Common mistakes: Memory failures, Overconfidence, We believe we are above average, Visual Detection, Vigilance Effectiveness.

Types of error

Human error rates and measurement

Trending and tracking


CAPA effectiveness

Learning Objectives

Understand human error: factors and causes.

Understand the importance: regulatory and business.

Define the process to manage Human Error deviations.

Identify Root Causes associated to human error deviations.

Learn how to measure human error rates at your site.

Identify what I can do to support human reliability.

Who Will Benefit

GMP regulated manufacturing facilities including pharma medical devices, biologics, food and nutrition and any other organization that have employees executing activities in which they can make mistakes (ALL).

For More Info, Please Click below URL:

Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.