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Sampling Plans for Risk Management in Incoming QC Usa 2017 webinar by Compliance4all

 
  November 17, 2016  
     
 
Compliance4All, Online
2017-01-24


Overview:
The pros and cons of the 2 most widely used sampling plans (ANSI Z1.4, 

and Squeglia's C=0) are examined in detail, focusing especially on the 

weaknesses of such plans in regards to meeting regulatory requirements. 

Real-world examples are provided for how using such sampling plans 

leads to production of non-conforming product. 

Why should you Attend: 
Almost all manufacturing companies spend time and money to inspect 

purchased parts upon receipt, in order to evaluate part quality before the 

parts Supplier is paid. "AQL" sampling plans are used almost universally 

for such inspections. However, AQL plans actually provide very little 

information about part quality.

Areas Covered in the Session:
    AQL and LQL sampling plans
    OC Curves
    AOQL
    ANSI Z1.4
    Squeglia's C=0

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




 
 
Organized by: Compliance4All
Invited Speakers:
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. 
 
Deadline for Abstracts: 2017-01-23
 
Registration:
Contact Detail:

Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com
http://www.compliance4all.com/
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E-mail: support@compliance4All.com
 
   
 
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