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    Webinar on Confidence-Reliability Calculations and Statistically Valid Sample Sizes

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    Website http://bit.ly/1ltrknK | Want to Edit it Edit Freely

    Category Webinar, Health, Medical, Pharma, Clinical

    Deadline: June 24, 2014 | Date: June 24, 2014

    Venue/Country: usa, U.S.A

    Updated: 2014-04-22 14:09:42 (GMT+9)

    Call For Papers - CFP

    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.

    Next, detailed descriptions are given for how to calculate confidence/reliability for data that is either pass/fail (i.e., "attribute" data), normally-distributed measurement data, non-normally distributed measurement data that can be transformed into normality, or non-normally distributed measurement data that cannot be transformed into normality. Spreadsheets are shown as examples of how to implement the methods described in the webinar. A final discussion is provided on how to introduce the methods into a company.

    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. The most informative method for analyzing the data that results from such activities is the calculation of the product's or lot's "reliability" at a chosen "confidence" level (where "reliability" means "in-specification"). Such a method produces information that is more valuable than simply that the given product or lot "passed" (as is the case when "AQL Attribute Sampling Plans" are used) or a % in-specification statement without any corresponding confidence statement (as is the case with AQL Variables Sampling Plans and with Process Capability calculations).

    The output of a "Confidence/Reliability" calculation is a definitive statement that the given product or lot has a specific % in-specification, which conclusion we can state with a specific level of confidence (e.g., 95% confidence of 99% reliability, or 90% confident of 93% reliability").

    Areas Covered in the Session:

    Regulatory Requirements

    Vocabulary and Concepts

    Attribute Data

    Normal Data

    Normal Probability Plotting

    Non-Normal Data that can be normalized

    Reliability Plotting (for data that cannot be normalized)

    Implementation Recommendations

    Who Will Benefit:

    QA/QC Supervisor

    Process Engineer

    Manufacturing Engineer

    QC/QC Technician

    Manufacturing Technician

    R&D Engineer

    Quick Contact:

    GlobalCompliancePanel

    USA Phone:800-447-9407

    webinarsatglobalcompliancepanel.com

    http://www.globalcompliancepanel.com

    Event Link - http://bit.ly/1ltrknK


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.