Human Error and Cognitive Load: How to Reduce Memory and Attention Failures
Instructor:
Ginette M Collazo
Product ID: 704210
- Duration: 60 Min
Why Should You Attend:
Attention and memory failures are usually associated to cognition overload. Slips, mistakes and decision making mishaps can be predicted, prevented and reduced. In this webinar we’re going to explore the human mind, human factors and cognitive overload as it associates with human error in GMP related environments. Some items that we will discuss include stress, task complexity, available time, fatigue, and other categories. This knowledge is to be applied to risk assessment, root cause analysis and CAPA development.
Areas Covered in the Webinar:
- Types of human error
- Taxonomy of human error
- 80/20 and human error reduction initiatives
- Individual performance
- Cognitive load and human error
- Cognitive load categories
- Importance and recommendations
Who Will Benefit:
- Training managers and coordinators
- Operations
- Manufacturing
- Plant engineering
- QA/QC staff
- Process excellence/improvement professionals
- Industrial/process engineers
- Compliance officers
- Regulatory/legislative affairs professionals
- General/corporate counsel
- Executive management
Ginette M Collazo
Organizational Psychologist, Ginette M Collazo Inc
Ginette Collazo, PH.D, is a human error and human behavior expert. She has spent more than 15 years in technical training, organizational development and human reliability areas. She has worked with Bristol-Myers Squibb, Johnson & Johnson, Schering-Plough, Wyeth, and has been a consultant with major firms like Abbott, Johnson & Johnson, Perrigo, among many others. She has also implemented human error reduction programs and technology in many small and mid-sized drug and device companies. An active researcher in specialized studies related to human reliability, she is the author of numerous publications on these topics.
Frequently Asked Questions:
- Are there GMP companies using the subject tool during their investigations?
More Training By Experts
- Human Error Reduction in GMP Manufacturing
- How to Write Error Free and FDA Compliant Procedures
- Human Error Investigations, Root Cause Determination and CAPA Effectiveness
- Precision Tools for Error Reduction: Strategies and Implementation Techniques
- Creating and Maintaining an Effective and Efficient Technical Training Programs
Refund Policy
Our refund policy is governed by individual products and services refund policy mentioned against each of offerings. However in absence of specific refund policy of an offering below refund policy will be effective.
Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange. Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time. On-Demand Recording purchases will not be refunded as it is available for immediate streaming. However if you are not able to view the webinar or you have any concern about the content of the webinar please contact us at below email or by call mentioning your feedback for resolution of the matter. We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email [email protected] call +1-888-717-2436 (Toll Free).
