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2 Day Seminar Reduce Human Error on the Drug and Device Manufacturing Proce...
Thu, March 23, 2017, 8:00 AM – 5:00 PM EDT
2 Day Seminar
Reduce Human Error on the Drug and Device
12 RAPS CREDITS
Location 1: 23- 24 Mar, 2017 Philadelphia
Location 2: 04- 05 May, 2017 New Brunswick
Call our customer care to get the Hotel details 844-267-7299
An Interative Workshop Presented BY WCS & Ginette M. Collazo PHD
This interactive workshop teaches you how to reduce your manufacturing error rates by 50%.
Course has been pre-approved by RAPS as eligible for up to 12 credits towards a participant’s RAC recertification upon full completion
Each attendee will receive 2 Day workshop materials by the speaker Seminar Also Includes Certificate, Complimentary Breakfast, Lunch & High Tea/Coffee provided by WCS.
Dr. Ginette Collazo — a 15 year veteran of helping drug, biologic and device firms reduce manufacturing errors by 50 percent or more — will conduct a one-of-a-kind workshop that teaches quality managers and manufacturing excellence professionals how to reduce errors and improve quality metrics.Dr. Collazo recently worked with a drug manufacturer that had a baseline rate of 4.7 errors per thousand units manufactured. But with effective human error reduction strategies, the error rate was reduced to 1.9.
A 60% reduction achieved in just 10 months
Human error is known to be the major cause of quality and production losses in many industries. Although it is unlikely that human error will ever be totally 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 behaviour CAN be manipulated reducing the likelihood of these occurrences. To work with these challenges it is really important to understand human behaviour and the psychology of error as well as understand exactly where the systems weaknesses are, so they can be improved and/or fixed. This course offers practical approaches to address human performance issues in GMP related environments by using a specific methodology to investigate, correct, prevent and avoid re-occurrence of these issues.
Free documents for Attendee:
RCDT – Root Cause Determination Tool
HE Assessment Template
Introduction of Tools Material
We will discuss human error categories, near root causes and root causes for these events. We will discuss latest trends in human error issues in the industry.
Meet Your Instructor:
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. Also has implemented human error reduction programs and technology in many more small and midsized drug and device companies. An active researcher in specialized studies related to human reliability, she is the author of numerous publications on these topics.
TRAINING WILL BENEFIT :
- Training managers and coordinators
- Plant engineering
- QA/QC staff
- Process excellence/improvement professionals
- Industrial/process engineers
- Compliance officers
- Regulatory/legislative affairs professionals
- General/corporate counsel
• Background on Human Error Phenomena
• Importance of Human Error Prevention/reduction
• Training and human error
• Facts about human error
• Human Error as the Root Cause
• What is Human Error
• How is Human Error controlled?
• Common mistakes: Memory failures, Overconfidence, We believe we are above average, Visual
Detection, Vigilance Effectiveness. Types of error
• Human error rates and measurement
• Trending and tracking
• CAPA effectiveness
Date and Time
DoubleTree by Hilton Philadelphia Airport ,4509 Island Avenue,
Location 1: 23- 24 Mar, 2017 Philadelphia / Location 2: 04- 05 May, 2017 New Brunswick
Philadelphia, PA 19153