Statistical Quality Control in Pharmaceutical and (IVD Industries)
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Website https://www.compliance4all.com/control/w_product/~product_id=502227LIVE?channel=ourglocal_Dec_2018_S |
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Category Clinical Labs, Translational research, Diagnostic Labs
Deadline: December 03, 2018 | Date: December 05, 2018
Venue/Country: Online, U.S.A
Updated: 2018-10-08 14:39:33 (GMT+9)
Call For Papers - CFP
Overview:Process validation is the establishment of documented evidence which provides a high degree of assurance that a specific process will consistently produce a product meeting its pre- determined specifications and quality characteristics.Areas Covered in the Session:The first step in establishing the control chart is to set the QC limits. The formula "Mean +/- 3*SD" is often taken for granted, the webinar will explain how the QC limits should be established. Why Mean?Why 3?Why SD?Why are the upper and lower limits symmetric around the mean?What N should be required to do this calculation?Who Will Benefit:Clinical LabsTranslational researchDiagnostic LabsLab CROCMCQuality ControlSpeaker Profile:Dr. Shuguang Huang has 20 years of experience working in pharmaceutical and diagnostic companies. He had assumed technical and management positions at Eli Lilly, Wyeth, Pfizer, and Precision Therapeutics, a cancer diagnostic company. In 2014, he co-founded and assumed the Chief Scientific Officer position for the statistics consulting company Stat4ward LLC. Event Fee: One Dial-in One Attendee Price: US$150.00Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: supportcompliance4All.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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