Why is it that the main users of Know Error are those Urology groups that do their own pathology???
These groups have COMPLETE control of the specimen from the time it leaves the patient until the time the pathology report is issued. If they can get a patient to sign the envelope containing the swab, do you think maybe they can get the patient to sign the sealed container enclosing their specimens?
Could it be that the Urologists don't know much about Pathology processes and that their hired Pathologists can't take responsibility for designing a process that is not really theirs in the first place? Why don't the companies that offer lab-in-the-box solutions offer quality process specimen identification procedures as well?
Maybe its just too much to ask for conscientious professional dedication when the activity is done for profit rather than for the benefit of the patient?