I am thinking there has to be a way to integrate the Validation into the 
Optimization the vendor does. I think you should be able to make microarray 
blocks/slides of at least 10 positive and more for ERPR per CAP during the 
optimization. Now, the vendor will say they only do Optimization, but there 
this is a way to get  them to do the stains for you at least. You can create 
your own document for the Validation. 
When your manager negotiates the cost of the analyzer, see if the vendor can 
help out with the initial expense with an allowance. It sounds like you might 
be past this point. 
Has anyone else done it this way?

Robert A. Eytalis
Laboratory Manager
robert-eyta...@riversidehealthcare.net
Phone: (815) 935-7256 ext. 5186
                (815) 935-7535
Fax         (815) 935-7068

Riverside Medical Center
350 N. Wall Street - Kankakee, IL 60901


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________________________________________
From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] on behalf of Fawn Bomar 
[fawn.bo...@halifaxregional.com]
Sent: Tuesday, October 01, 2013 12:06 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Validating new Benchmark instrument

Hi everyone,



I know that this subject has come up several times and I am sorry to bother 
everyone again but I was hoping to find some help.  We are upgrading our 
Benchmark Immuno machines to the Benchmark XT immuno machine at the end of 
October.  Does anyone have any suggestions on how to approach the validation 
process?  Do we need to validate every antibody that we use as well as the 
kits?  I know that there is also a gray area surrounding how many slides need 
to be run to consider the antibody validated, but what would be the suggested 
amount of slides to validate a new machine as I know this will be very costly.  
Does anybody have a log/checklist/spreadsheet that they would be willing to 
share to help document this validation of the machine and each of the 
antibodies?



Thank you in advance for your help



Fawn Bomar
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