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    HEALTHCARE TRAINING 2021 - Preventing Human Error in the Life Sciences

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    Website https://www.compliance4alllearning.com/webinar/preventing-human-error-in-the-life-sciences-503840LIV | Want to Edit it Edit Freely

    Category HEALTHCARE TRAINING 2021

    Deadline: July 07, 2021 | Date: July 07, 2021

    Venue/Country: Online event, U.S.A

    Updated: 2021-05-31 20:15:52 (GMT+9)

    Call For Papers - CFP

    Overview:

    This webinar will explore the true causes and nature of human error, how human error should be investigated, how human error relates to human performance, and the difference between real human error and systems, process, and management deficiencies.

    Why you should Attend: Human Error occurs in all settings. In the world of pharmaceutical manufacturing, the result of that error can result in loss of product or at the most extreme, injury to patients. Human is a frequent occurrence in pharmaceutical manufacturing. It occurs even when every obvious preventive actions have been employed such as effective compliance documentation development and training.

    Unfortunately, sometimes these actions are not adequate to prevent these errors from occurring. "Human Error" is sometimes not the cause of issues even though relegated/assigned as the root cause of adverse events with reasons assigned such as "lack of attention to detail" or "failure to follow procedure." Corrective action in these instances often involve re-training or disciplinary action.

    These approaches do not seek to understand really why the error(s) occurred.

    Areas Covered in the Session:

    What is Human Error?

    Nature of human error in pharmaceutical manufacturing

    Approaches to investigating Human Error

    The root causes that are directly attributable to Human Error

    The role of leadership in Human Error reduction

    Human Error Reduction Strategies

    Human Error Prevention and Reduction Drivers

    Who Will Benefit:

    Manufacturing

    Engineering

    Quality

    Regulatory functions or Services to include

    Machine Operators and Mechanics

    Quality Assurance

    Technical Services

    Laboratory

    Regulatory

    Engineers

    Documentation development and management with titles such as Associates, Technicians, Scientists, Supervisors, Managers, and Directors

    Speaker Profile

    Charles H. Paul is the President of C. H. Paul Consulting, Inc. - a regulatory, manufacturing, training, and technical documentation consulting firm - celebrating its twentieth year in business in 2017. He has been a regulatory and management consultant and an Instructional Technologist for 30 years and has published numerous white papers on various regulatory and training subjects. The firm works with both domestic and international clients designing solutions for complex training and documentation issues.

    He has held senior positions in consulting and in corporate training development prior to forming C. H. Paul Consulting, Inc. He also worked for several years in government contracting managing the development of significant Army-wide training development contracts impacting virtually all of the active Army and changing the training paradigm throughout the military.

    He has dedicated his entire professional career explaining the benefits of performance-based training


    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.