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Re: To Luxel Users
- To: sandyfl <sandyfl@earthlink.net>
- Subject: Re: To Luxel Users
- From: John R Laferriere <John.R.Laferriere@dupontpharma.com>
- Date: Tue, 28 Mar 2000 13:54:20 -0500
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- Cc: radsafe <radsafe@romulus.ehs.uiuc.edu>
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Sandy wrote (in part):
One might also ask, if the regulatory limits are 1250 mrem/qtr, or,
5000 mrem/yr (TEDE), why measure dose at 1 mrem at all, even if
this can be attributed to occupational exposure? In my opinion,
reporting and recording dose down to 1 mrem "gives significance to
the insignificant."
The relevance or value of reporting doses down to one millirem (0.01 mSv) is indeed a matter of opinion, (technical
issues aside). However, the 1 mrem reporting level is one of the unique capabilities of Luxel, and one which
appears to be an important feature from a marketing standpoint. Many customers will see value in the 1 mrem reporting
level, and in being able to get a dose report that says 35 instead of 30 or 40. It does seem to be a net improvement in
dosimetry capability to be able to measure doses that low. So when Sandy disparages the 1 mrem capability as
"giving significance to the insignificant", it smacks of either sour grapes or an attempt to minimize the significance of
a competitor's unique product features. I have no problem with anyone NOT employed at a dosimetry vendor voicing
this opinion, but people in Sandy's position should be aware that they have a higher standard to meet to protect their
reputation as a technical resource so they do not appear to be wearing a "marketing" hat part time while posting to radsafe.
Regards,
John R. Laferriere, CHP
DuPont Pharmaceuticals Co.
Medical Imaging Division
john.r.laferriere@dupontpharma.com
(978) 671-8316 fax (978) 671-8149