This should help...the IHC "test" is the pathologists' INTERPRETATION of IHC 
stain.  The stain procedure, validation of protocols and controls, and lot to 
lot validation must be signed off by a pathologist.
 Any tech that has demonstrated competency in performing the procedure, can 
perform IHC staining. Any tech can also perform an antibody work-up, provided 
the "results" are signed off by a pathologist.
Easy-peasy

Terri L. Braud, HT(ASCP)
Anatomic Pathology Supervisor
Laboratory
Holy Redeemer Hospital
1648 Huntingdon Pike
Meadowbrook, PA 19046
ph: 215-938-3689
fax: 215-938-3874

-----Original Message-----

   4. Personel (Jesus Ellin)
----------------------------------------------------------------------
Message: 4
Date: Tue, 22 Nov 2016 17:36:20 +0000
From: Jesus Ellin <jel...@yumaregional.org>
Subject: [Histonet] Personel
So I know I am going to open Pandoras box,, but have people been paying 
attention to the Personal requirements from CAP.

I called the CAP and asked them about the criteria concerning Moderate or High 
complexity testing, after discussing with them the situations,   IF you have a 
tech that is Licensed and Also has a QIHC, but does not minimum requirement 
Defined by CLIA in education ,, they CAN NOT do any QA/OC of IHC and antibody 
work up,, as IHC is defined as High complexity testing.

I also asked about the test systems.  The grandfather clause is only good for 
test systems that occurred for those time periods.  For instance if CLIA 
defined the test system after those dates of 1997,, then they are not included 
and the person cannot perform test and technology created after those dates, 
since the testing was not in place during the grandfather clause time.  In a 
nut shell meaning if the IHC staining and antibody was developed after those 
dates,, you are not covered by the grandfather clause to do the testing ,, can 
some help clear this up,,

So any help on this matter will do




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