Place : United States, Aurora
Contact Person:Training Doyens
Description:Understand the root causes for human error deviations and techniques of human error reduction. The webinar also explains CAPA, and investigation procedures in GMP regulated industry.
Deadline for abstracts/proposals : 6th August 2019
Organized By :Training Doyens
Keynote Speakers : Years of Experience: 23+ years Areas of Expertise: Engineering Psychology and Human Reliability 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. 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,
Venue :26468 E Walker Dr, Aurora, Colorado 80016, USA
Check the event website for more details.