This bundle contains 3 Pharmaceutical On-Demand webinars at a discounted price of 50% Each webinar is 1.5 hours in length. Registrations include Three months of OnDemand playback.These webinars are entirely presented by our Pharmaceutical Expert Ginette Collazo.
In pursuing perfection, organizations endeavor to minimize human error within their operational frameworks. Achieving a Human error-free environment is a complex goal. While achieving absolute error-free systems remains elusive, various strategies and approaches can significantly mitigate human error in diverse environments.
Understanding the nature of human error is fundamental. Humans, by nature, are imperfect beings susceptible to mistakes due to factors like fatigue, stress, cognitive biases, and inadequate training. Acknowledging these inherent limitations is the first step toward devising effective strategies.
Webinar Highlights:
Why Should You Attend:
Human error is the primary cause of quality and production losses in many industries. Although human error is unlikely to be eliminated, many human performance problems can be prevented. Human errors start at the design stage. From procedures, training, supervision, and workplace environment, many variables that affect human behavior can be manipulated to reduce the likelihood of these occurrences. To work with these challenges, it is essential to understand human behavior and the psychology of error and know precisely where the system's weaknesses are so they can be improved and fixed.
Who Should Attend:
Human error is known to be the primary cause of quality and production losses in many industries. Although it is unlikely that human error will ever be eliminated, many human performance problems can be prevented. Human errors start at the design stage. Procedures play a vital role in human reliability. Nevertheless, it is essential to understand human behavior and the psychology of error as well as understand exactly where the instruction's weaknesses are so that procedures can be human-engineered, improved, and fixed.
Areas Covered:-
Why You Should Attend:-
Procedures account for more than 40% of human error events in manufacturing. The majority of regulatory citations are also related to procedures. Procedures are essential for both execution and audits. These should be written for users without missing relevant information for regulators. Usually, procedures have weaknesses that harm productivity, quality, and regulatory standing. We will discuss content development to formats designed for human error reduction due to procedures.
Who Will Benefit:-
Human error is known to be the primary cause of quality and production losses in many industries. Although it is unlikely that human error will ever be 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. When working with these challenges, it is imperative to understand human behavior and the psychology of error as well as understand exactly where the weaknesses of the system are so that they can be improved and fixed. This course offers practical approaches and tools to address human performance issues in GMP-related environments by using a particular methodology to correct, prevent, and avoid the reoccurrence of these matters.
Areas Covered:-
Key Learning Objectives:-
Who will benefit?