Ginette Collazo, Ph. D. is an Industrial-Organizational Psychologist with 20 years of experience that specializes in Engineering Psychology and Human Reliability, disciplines that study the interaction between human behavior and productivity. She has held positions leading training and human reliability programs in the Pharma Read more
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 reoccurrence of these matters.
Course Objectives:
• Understand human error: factors and causes.
• Understand the importance: regulatory and business.
• Define the process to manage Human Error deviations.
• Learn about human error measurement.
• Learn about tools for measurement.
• Establish Key Performance Indicators.
• Define and measure human error rate, cognitive load, and CAPA effectiveness
• Identify what I can do to support human reliability.
Course Outline:
• Background on Human Error Phenomena and Measurement.
• The importance of Human Error Prevention/reduction.
• Quantitative and qualitative information gathering.
• Why do we need tools for human error reduction programs?
• Training as a tool and human error.
• Facts about human error and training.
• Human Error as the Root Cause: what to do and how to measure it.
• Tools
o Prediction
o Root Cause Analysis
o Cognitive load assessment
o Systems available
o Human error rate
o Floor checklist
o Interview questions
• Human error rates and other metrics
• Trending and Tracking
• Metrics and Human Error
o KPI’s
o Human Error rate
o 1st-time pass rate
o Overall equipment effectiveness (OEE)
o Trending /Tracking
What You Get:
• Training Materials
• Live Q&A Session with our Expert
• Participation Certificate
• Access to Signup Community (Optional)
• Reward Points
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
Write it Right – Well Written Procedures are Essential for QMS Effectiveness
LIVE : Scheduled on
07-November-2024 :01:00 PM EST
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6-Hour Virtual Seminar - Death by CAPA - Does your CAPA Program need a CAPA?
LIVE : Scheduled on
19-November-2024 :11:00 AM EST
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4-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries (Pharma, Biotech, Devices, etc-)
LIVE : Scheduled on
21-November-2024 :01:00 PM EST
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Verification and Validation – Product, Process or Equipment and QMS Software
LIVE : Scheduled on
22-November-2024 :01:00 PM EST
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Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configuration
LIVE : Scheduled on
25-November-2024 :01:00 PM EST
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