Brian,

Under some Annexes of the European Directives, such as the Meduical Devices
Directive and the RTTE Directive, ISO 9K and/or 2K is a requirement.



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PETER S. MERGUERIAN
Technical Director
I.T.L. (Product Testing) Ltd.
26 Hacharoshet St., POB 211
Or Yehuda 60251, Israel
Tel: + 972-(0)3-5339022  Fax: + 972-(0)3-5339019
Mobile: + 972-(0)54-838175
http://www.itl.co.il
http://www.i-spec.com





-----Original Message-----
From: Brian O'Connell [mailto:[email protected]]
Sent: Thursday, August 08, 2002 4:36 PM
To: Product Safety Technical Committee
Subject: ISO 9k/2k relevance



Good People of the PSTC:

I've had some conversations with our Component Engineers, Sales and QA
people. I could not identify any customer that placed an order based on our
ISO 9k and/or 2k certification.  Nor could I identify any component
specified and/or purchased that was based on whether a supplier has ISO
certification.

Is the ISO "paper mill" relevant? Is there empirical evidence that ISO
certification results in "better stuff"?  Is ISO certification a requirement
for your purchasing policies? Has ISO certification been a determining or
contributing factor for selection of your company's products?

At this point, I am not being critical of the ISO "process"; I am attempting
to understand its ROI and relevance to product quality.

I speak only for myself; nothing said here represents my employer's
policies.

R/S,
Brian


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