Organization Name / Organize By
AtoZ Compliance
Organizing/Related Departments
Controlling Human Error
Organization Type
Organization/Company
WebinarCategory
Both (Technical & Non Technical)
WebinarLevel
All (State/Province/Region, National & International)
Related Industries
Biotechnology
Medical/Healthcare/Hospital
Location
New York, United States
Key Take Away
This course offers practical approaches and models to address human performance issues in GMP related environments by using a specific methodology to correct, prevent and avoid re-occurrence of these issues.
Overview
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 behavior CAN be manipulated reducing the likelihood of these occurrences. To work with these challenges it is really important to understand human behavior and the psychology of error as well as understand exactly where the systems weaknesses are, so they can be improved and/or fixed.
Why Should You Attend
This training would provide tools that can be implemented and used after this event. This includes practical tools. 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.
Areas Covered In This Webinar
- 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
- Prediction
- CAPA effectiveness
Learning Objectives
- Understand human error: factors and causes.
- Understand the importance: regulatory and business.
- Define the process to manage Human Error deviations.
- Identify Root Causes associated to human error deviations.
- Learn how to measure human error rates at your site.
- Identify what I can do to support human reliability.
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
Email: [email protected]
Toll Free: +1- 844-414-1400
Tel: +1-516-900-5509
Fax: +1-516-300-1584
Others Details
This root cause analysis training offers practical approaches and models to address human performance issues in GMP related environments. Book now!
Registration Fees
Available
Registration Fees Details
Live Webinar- $199 i
for one participant
Live Webinar-Corporate- $549 i
Any Number of Participants from one Location
Recorded Webinar- $219 i
Get access to the webinar recording link for 6 months
Webinar Training CD- $399 i
Get life time access to webinar for unlimited participants
Registration Ways
Email
Phone
Website
Post Box
Other