Minimizing Human Error
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How To Reduce Human Error In Manufacturing
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Human Error Reduction Tools
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Pricing Options QMS for Every Business Size Calculating ROI IT Resource Considerations Medical Device Solutions Design Control Device History Records ways to prevent human error Medical Device Reporting (eMDR) Pharmaceutical Solutions Clinical Management Trial Master File (eTMF) Regulatory Management Submissions Management COMPLIANCE Stay On Top of Ever-Changing Regulations and Quality Standards Find Out How FDA 21 CFR 21 http://www.facilitiesnet.com/datacenters/article/How-to-Minimize-Human-Error-Prevent-Data-Center-Downtime-Facilities-Management-Data-Centers-Feature--14223 CFR Part 11 21 CFR Part 111 21 CFR Part 1270-1271 21 CFR Part 210-211 21 CFR Part 606 21 CFR Part 820 ISO ISO 9000 ISO 9001 ISO 13485 ISO 14000 ISO 14971 ISO 15189 ISO 17025 Other Regulations & Standards TS 16949 CLIA Canadian Standards EU Annex 11 Need Help With Compliance Quality & Compliance Consulting RESOURCES Get Best Practices, Industry Insights, Solution Demos and More http://www.mastercontrol.com/newsletter/pharmaceutical/reducing_human_error_manufacturing_floor_0310.html Find Out How Resource Center White Papers Case Studies Testimonials Blog - GxP Lifeline ABOUT US The #1 Enterprise Quality Management Software (EQMS) since 1993 See What We Do Company Info Who are we? Contact Us Careers News & Events Our Team Executive Team Partners For Pharmaceuticals and Biotechnology Reducing Human Error on the Manufacturing FloorBy Ginette M. Collazo, PhD. Jun 15, 2010 | Free Downloads | | As technology advances, human error in manufacturing becomes more and more visible every day. Human error is responsible for more than 80 percent of process deviations in the pharmaceutical and related manufacturing environments. Sadly, little is known about the nature of these events mainly because quality event investigations end where human error investigations should begin. Human error is about explaining human behavior. Chemical engineers explain product behavior, mechanical engineers explain equipment behavior, industrial engineers explain process behavior, but who explains human behavior? When we investigate quality events, the focus of those investigations rely on explaining what happened in the process and how the product was affected. A human error usually explains the reason for the occurrence of the deviation; nevertheless, the reason for that error remains unexplained and consequently the corrective
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