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EVENT DATES
Jan 2017
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Webinar on Process Capability Analysis by means of Confidence

Online Event

Overview

Overview:
The webinar begins with a discussion of relevant regulatory requirements, as motivation for calculating "confidence/reliability". Then, some vocabulary and basic concepts are discussed.

Why should you Attend:
All manufacturing and development companies perform testing and/or inspections that involve concluding whether or not a product or lot is acceptable vs. design or QC specifications. Such test/inspections may occur during design verification/validation or during incoming or final QC.

Areas Covered in the Session:
    Regulatory Requirements
    Vocabulary and Concepts
    Attribute Data
    Normal Data
    Normal Probability Plotting

Who Will Benefit:
    QA/QC Supervisor
    Process Engineer
    Manufacturing Engineer
    QC/QC Technician
    Manufacturing Technician
    R&D Engineer

Speaker Profile:
John N. Zorich has spent 35 years in the medical device manufacturing industry; the first 20 years were as a "regular" employee in the areas of R&D, Manufacturing, QA/QC, and Regulatory; the last 15 years were as consultant in the areas of QA/QC and Statistics. His consulting clients in the area of statistics have included numerous start-ups as well as large corporations such as Boston Scientific, Novellus, and Siemens Medical.

Contact Detail:

Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com
http://www.compliance4all.com/
Event Link : http://www.compliance4all.com/control/w_product/~product_id=501098LIVE?channel=mailer&camp=Webinar&AdGroup=eventsinamerica_Jan_2017_SEO
Twitter Follow us – https://twitter.com/compliance4all    
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LinkedIn Like us – https://www.linkedin.com/company/compliance4all

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