Preventing Human Error in the Life Sciences

  • Speaker:Charles H. Paul
  • Date: 23rd August 2018 10:00 AM PST | 01:00 PM EST
  • Duration:60Min
  • Product Code:GRC-90374

$169

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If you are unable to attend the meeting Live then you can opt in for the Live Recording instead. Access the Recording of the Training for 6 months. Contact our support for any questions. To prepare an invoice to pay by Check or Wire email us at support@grcts.com. 


Certification - GRCTS Attendance Certificate

Background:      

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 must 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:            

This webinar will benefit everyone in the life sciences who works within the manufacturing, engineering, quality, and 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.         

This webinar applies to all worker levels – associates, managers, directors, vice presidents

  • Packaging engineers
  • Operations personnel
  • Regulatory associates
  • Medical device research and development associates, scientists, managers and directors
  • Quality assurance and quality control personnel in the medical device industry
  • Compliance managers and directors

Instructor Profile:

Charles H. Paul is the President of C. H. Paul Consulting, Inc. – a regulatory, training, and technical documentation consulting firm.  Charles has been a regulatory consultant for over 20 years and has published numerous white papers on the subject.  The firm works with both domestic and international clients designing solutions for complex training and documentation issues.

Available Options

Live Meeting Access Single: Attend the meeting Live via Webex Meeting

$169

2 Single Live Access: 2 people can attend the meeting Live from any location

$279

Recording: Access the training Recording for 6 months from any location

$249

CD: Shipped within 2 working days

$359

USB - Shipped within 2 working days

$379

Live + Recording: Attend Live Meeting Online + Access the recording for 6 months

$289

Live + CD: Attend Live Meeting Online + Get the training CD shipped for free

$389

Live + USB - Attend Live online + Get the training USB shipped for free

$409

5 Member Group: 5 can Attend Live Meeting Online from any location globally

$539

10 Member group: 10 can Attend Live Meeting Online from any location globally

$839

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