Place : United States, Aurora
Contact Person:Training Doyens
Description:Understand what human error is and how to implement an effective human error reduction program for improving efficiency as well as complying with FDA regulations.
Deadline for abstracts/proposals : 4th June 2019
Organized By :Training Doyens
Keynote Speakers : 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 Pharmaceutical and Medical Device Manufacturing Industry.
Conference Highlights :OVERVIEW 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
Venue :26468 E Walker Dr, Aurora, Colorado 80016, USA
Check the event website for more details.