52: What does the FDA say about non-clinical digital pathology for GLP?

Send us a text Several scanners have been cleared by the FDA for clinical pathology work, but what about FDAs stand on all the nonclinical pathology work done in a regulatory environment? Specifically the work done in the Good Laboratory Practice (GLP) compliant environment? Can we use the slides without restrictions in lieu of glass slides?What part of the digital pathology system do we need to validate?How do wemaintain and archive the whole slide images used for the pathology portion of th...