Hi histoland,

I am exploring digital pathology and I am unclear about the current CAP 
requirements and how those may change if the platform is FDA approved for 
primary diagnosis.  Is the wash out period still necessary if it’s not 
considered and LDT?  Does the personnel still have to be qualified as high 
complexity testing personnel to scan the slides?  Any help or other information 
is greatly appreciated!

Thanks,
Cristi

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