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Report: The State of Quality in the Telecommunications Industry

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(QuEst Forum: Dallas) -- QuEST Forum unveiled its inaugural report on the state of quality in the telecommunications industry at the 2009 Asia Pacific Best Practices Conference, which was held Oct. 20–22 in Shanghai.

Kaizen by Inspiration is Not Kaizen

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I was flipping through some Japanese books on sayings and speeches given by Taiichi Ohno looking for inspiration for a new article when I found the following passage:

SGS Is the First and Only Registration Body Accredited to RIOS and R2 by ANAB

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(SGS: Rutherford, NJ) -- SGS announced that it is the first registrar in the world to be accredited to The Recycling Industry Operating Standard (RIOS) and The Responsible Recycling Standard (R2) by ANSI-ASQ National Accreditation Board (ANAB).

Baldrige Award Application for 2010 Available

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(NIST: Gaithersburg, MD) -- Eligibility and application forms for the Malcolm Baldrige National Quality Award are now available on the Baldrige web site.

Survey: North American Manufacturers Cite High Supply Chain Risk

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(MFG.com: Atlanta) -- More than one-third of North American manufacturers responding to MFG.com’s most recent MFGWatch survey say they’ve experienced a significant supply chain disruption in the past three months, and more than 70 percent indicate they plan to maintain or increa

Product News: Game Makes Quality Concepts Fun to Learn

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Product News: Blue Light LED Flashlight Safe for NDT Inspection

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(Spectronics Corp.: Westbury, NY) -- Spectronics Corp. has introduced the

Quality Insights: How Do Sampling Plans and AQLs Work?

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If you are buying two or three complex assemblies per month from a contract manufacturer, it would be reasonable to check every one carefully; there’s a lot that could go wrong.

Scientists Build First ‘Frequency Comb’ To Display Visible ‘Teeth’

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(NIST: Gaithersburg, MD) -- Finally, an optical frequency comb that visibly lives up to its name.

Electronic Medical Device Reporting Best Practices

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The FDA’s Center for Devices and Radiological Health (CDRH) posted a notice of draft guidance that will require all medical device adverse-event reports to be submitted electronically.

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