THIS ROOT CAUSE ANALYSIS TRAINING OFFERS PRACTICAL 2017 - Tools for Human Error Reduction -By AtoZ Compliance

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Category fda 510k training, form fda 3632, fda gmp training, fda pre-approval inspection checklist, fda environmental monitoring, medical device quality system webinar, training fda medical devices, medical coding compliance plan, fda medical device training, capa system, fda guidance human factors, human error prevention, human factors fda guidance, human resources measurement and metrics, root cause analysis training

Deadline: June 13, 2017 | Date: June 13, 2017

Venue/Country: Online, U.S.A

Updated: 2017-05-29 20:23:03 (GMT+9)

Call For Papers - CFP

This root cause analysis training offers practical approaches and tools 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.

Why Should You Attend:

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.

Areas Covered In This Webinar:

Background on Human Error Phenomena and measurement.

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

Prediction

Root Cause Analysis

Cognitive load assessment

Systems available

Human error rate

Floor checklist

Interview questions

Human error rates and other metrics

Trending and tracking

CAPA effectiveness

Metrics and Human Error

KPI’s

Human Error rate

1st time pass rate

Overall equipment effectiveness (OEE)

Trending /Tracking

Learning 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.

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

For more information, please visit : http://bit.ly/2qUkjE6

Email: supportatozcompliance.com

Toll Free: +1- 844-414-1400

Tel: +1-516-900-5509

Speakers Profile:

Ginette M. Collazo, Ph.D

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 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.