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> It seems to me that you have a 21CFR820 compliance problem if you can't
> cross-check your document revisions against their associated device
Yeah, it's hard for me to believe that a US medical device manufacturer
wouldn't have a tightly controlled process in place for releasing new
versions and their docs. Aside from the thousands of pages of regulations,
there are liability issues...
Richard G. Combs
Senior Technical Writer
richardDOTcombs AT polycomDOTcom
rgcombs AT gmailDOTcom
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