Human Error Reduction Program 2022 - How To Implement An Effective Human Error Reduction Program

How To Implement An Effective Human Error Reduction Program
Product Id : FDB3215
Category : Cross Functional, Food, Drugs & Biologics, Medical Devices, Quality
Presenter : Dr. Ginette Collazo
Scheduled On : May 05 2022 1:00 pm
US/Canada (Eastern Time - ET)
Duration : 90 Minutes
Attend this training to learn how to implement a Human Error Reduction Program at your site. It includes practical tools and explains how to measure effectiveness to continuously improve human reliability at your site.
Why You Should Attend:
If you work in the GMP regulated industry you not only need to address human error deviations because they are an inconvenience, you must do it because the regulation requires it. For example; The CFR – Code of Federal Regulations Title 21 Subpart B_Organization and Personnel Sec. 211.22 talks about the “Responsibilities of quality control unit.” and it states that “(a) There shall be a quality control unit that shall have the responsibility and authority to approve or reject all components, drug product containers, closures, in-process materials, packaging material, labeling, and drug products, and the authority to review production records to assure that no errors have occurred or, if errors have occurred, that they have been fully investigated…” Also, the European Commission reads “Where human error is suspected or identified as the cause; this should be justified having taken care to ensure that process, procedural or system-based errors or problems have not been overlooked if present.
Appropriate corrective actions and/or preventative actions (CAPAs) should be identified and taken in response to investigations. The effectiveness of such actions should be monitored and assessed, in line with Quality Risk Management principles.” We in Human Error Solutions have created the simplest and most effective human error reduction program, with 100% effectiveness when fully implemented in different organizations around the world. This valid scientific model combines qualitative and quantitative methodologies and provides practical tools that would assist your organization in achieving desired to results.
Learning Objectives:
Error Reduction System
6 Step Implementation Process
HES Tools
Implementing the program
Metrics and KPI’s
Areas Covered in the Session :
What is Human Error
How is Human Error controlled?
6 step method for error prevention
Human error rates and measurement
Trending and tracking
Prediction
Effectiveness
Who Should Attend:
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