Wednesday, February 25, 2015

Just released: FDA draft guidance: Technical Performance Assessment of Digital Pathology Whole Slide Imaging Devices

Technical Performance Assessment of Digital Pathology Whole Slide Imaging Devices



"Recent technological advances in digital microscopy, in particular the development of whole slide scanning systems, have accelerated the adoption of digital imaging in pathology, similar to the digital transformation that radiology departments have experienced over the last decade. The FDA regulates WSI systems manufacturers to ensure that the images produced for clinical intended uses are safe and effective for such "

HT:AR

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