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Live Webinar The prevention of human error in pharmaceutical manufacturing

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Website https://worldcomplianceseminars.com/webinardetails/393 | Edit Freely

Category

Deadline: August 01, 2018 | Date: August 03, 2018

Venue/Country: Online, U.S.A

Updated: 2018-05-04 13:09:08 (GMT+9)

Call For Papers - CFP

Live Webinar The prevention of human error in pharmaceutical manufacturing

Time: 01:00 PM EDT | 10:00 AM PDT | 12:00 PM CDT Duration 60 Minute

Description

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.

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. 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.

Price: $179 One Dial-in One Attendee | Corporate Live Recorded $279 One Dial In - Max 10 attendees |Group $695 Multiple locations upto 5 dial in | Recorded $349


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.