Reducing Bottlenecks In GxP Laboratories
Reducing Bottlenecks In GxP Laboratories With Electronic SOP Document And Workflow Systems In the QC laboratory, adherence to Good Manufacturing Practice (GMP) guidelines necessitates the need to maintain thorough documentation to ensure strict compliance with established procedures. Completing paper documents and ensuring their authenticity creates a burdensome bottleneck for the QC laboratory. This presentation will discuss strategies for using an electronic SOP document and workflow system to boost laboratory productivity. • Electronic SOP document and workflow systems improve SOP completion times, reduce procedural and transcription errors, and reduce review & sign-off times • A more efficient SOP documentation process translates into a more efficient documentation workflow, more accurate records, and faster product release. • An electronic SOP documentation system offers the opportunity to address the three major tenets of Lean Process manufacturing: eliminate waste, improve workflows, and improve quality. SPEAKER Chris Stumpf, Ph.D. Senior Product Marketing Manager, Informatics Waters Corporation Chris joined Waters in 2001 after earning his Ph.D. in Analytical Chemistry and Mass Spectrometry from Purdue University in 2000, and held a post doctoral position at the University of Cincinnati Medical School conducting proteomics research. During his doctorate and post-doctorate education, he became keenly interested in informatics solutions to manage and mine analytical data
- Presenting
- Chris Stumpf, Ph.D.
- Channel
- PFQ and Food Quality Webcast Channel
- Date
- Jan 19 2010
- Duration
- 3804
- Tags
- Waters, reducing, bottlenecks, GxP, Labs
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