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    Controlling human error in the manufacturing floor

    View: 138

    Website http://bit.ly/2oBgCzj | Want to Edit it Edit Freely

    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 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

    Prediction

    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:

    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

    Speaker 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/2oBgCzj

    Email: referralsatcomplianceglobal.us

    Toll Free: +1-844-746-4244

    Tel: +1-516-900-5515

    Fax: +1-516-900-5510


    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.