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Site language : English - Français
Ref : 27207
Event :Live Webinar The prevention of human error in pharmaceutical manufacturing

Date :Friday August 03rd, 2018

Location :Online (Internet, Videoconferencing, ...)

Type :Education - International audience

Accreditation :--


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Live Webinar The prevention of human error in pharmaceutical manufacturing





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 should you 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 occurrance 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

•    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 who works within the manufacturing function or services the function to include, machine operators and mechanics, quality assurance, technical services, laboratory, regulatory, documentation development and management with titles such as associates, technicians, scientists, supervisors, managers, and directors.



Industries who can attend

This 60-minute online course is intended for professionals in the Medical Device, Biotechnology,Pharmaceutical Industry. Although not presently stated in the draft , the same guide could be used by FDA Regulated Industries personnel.



Charles H Paul

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. Charles 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

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