Controlling human error in the manufacturing floor
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Category human error assessment and reduction technique, human error prevention, human error reduction, human factors fda, human factors fda guidance
Deadline: May 16, 2017 | Date: May 16, 2017
Venue/Country: New York, U.S.A
Updated: 2017-04-25 18:07:55 (GMT+9)
Call For Papers - CFP
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. 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 Human Error Prevention & Reduction webinar 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 will 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. Also, we will discuss latest trends in human error issues in the industry.Areas Covered in this Webinar:Background on Human Error PhenomenaImportance of Human Error Prevention/reductionTraining and human errorFacts about human errorHuman Error as the Root CauseWhat is Human ErrorHow is Human Error controlled?Common mistakes: Memory failures, Overconfidence, We believe we are above average, Visual Detection, Vigilance Effectiveness.Types of errorHuman error rates and measurementTrending and trackingPredictionCAPA effectivenessLearning 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:Training managers and coordinatorsOperationsManufacturingPlant engineeringQA/QC staffProcess excellence/improvement professionalsIndustrial/process engineersCompliance officersRegulatory/legislative affairs professionalsGeneral/corporate counselSpeaker Profile: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. For more detail please click on this below link:http://bit.ly/2oBgCzjEmail: referralscomplianceglobal.usToll Free: +1-844-746-4244Tel: +1-516-900-5515Fax: +1-516-900-5510
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