Re: [Histonet] Equipment Validation
I'm not familiar with the JCAO requirements, but I know a little about the
GLP requirements. Usually these requirements are mainly intended for
instruments that are reporting data. In anatomic path, the pathlogists are
the "instrument". I do think it is smart to test any new equipment that
comes into the lab to ensure it does what it is supposed to do.
Patti Loykasek
PhenoPath Laboratories
Seattle, WA
> Good morning everyone.
>
> I have a question concerning equipment validation.
>
> We recently had a customer that said they were cited during an inspection
> for not having a record of their new equipment being validated.
> I am assume that the validation of the equipment means that they should
> have run a parallel test with the new and "old" piece of equipment to
> verify that it indeed performs as it should. The customer felt it was our
> responsibility to do the validation testing in their lab for the equipment.
> Does anyone have some more insight or protocols as to what equipment
> validation documentation is required of inspecting agencies like Joint
> Commission ?
>
> I appreciate your input.
>
> Have a Blessed Day !
>
>
> Best regards,
>
> Mark
>
> Mark Lewis
> Product Specialist
> Anatomical Pathology
> Clinical Diagnostics
> Thermo Electron Corporation
> (412) 747-4013
> (412) 788-1097
> E-mail: mark.lewis@thermo.com
>
>
>
>
> _______________________________________________
> Histonet mailing list
> Histonet@lists.utsouthwestern.edu
> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
_______________________________________________
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet
<< Previous Message | Next Message >>