I think you will find that this dependant upon the product type and ISO 900
may not be sufficient.


Gregg Kervill DipIM, MIMgt, MIEEE

VP Engineering
Test4Safety.com Inc
PO Box 310,
Reedville, VA
22539. USA

Phone  ( 804) 453-3141
Fax        (804) 453-9039



------Original Message-----
-From: [email protected]
-[mailto:[email protected]]On Behalf Of
[email protected]
-Sent: Wednesday, June 19, 2002 10:25 AM
-To: [email protected]; [email protected]
-Subject: RE: ISO 9000
-
-
-
-Hello Martin,
-
-If you are a medical device manufacturer, to comply with the
-European Medical Device Directive, you have to have ISO 9000
-accreditation. Otherwise, ISO 9000 compliance is a
-market/customer requirement, not a regulatory requirement.
-
-Regards,
-+=================================================================+
-|Ronald R. Wellman                |Voice : 408-345-8229           |
-|Agilent Technologies             |FAX   : 408-553-2412           |
-|5301 Stevens Creek Blvd.,        |E-Mail: [email protected]|
-|Mailstop 54L-BB                  |WWW   : http://www.agilent.com |
-|Santa Clara, California 95052 USA|                               |
-+=================================================================+
-
-
------Original Message-----
-From: [email protected]
-[mailto:[email protected]]
-Sent: Tuesday, June 18, 2002 7:24 PM
-To: [email protected]
-Subject: ISO 9000
-
-
-
-Greetings,
-
-Several years ago most manufacturing companies were getting
-evaluated to
-ISO 9000 standards.  Since that time, there have been some
-revisions to the
-standards.  Does your company still spend time and money
-dealing with ISO
-9000 and it's revisions.  If so, why.  If not, why not?
-
-I realize this subject is not directly related to product
-safety/EMC, so,
-if you like,  you can email me directly with your responses.
-
-All responses are appreciated.
-
-Regards
-
-Joe Martin
-EMC/Product Safety Engineer
-Applied Biosystems
[email protected]
-
-
-
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