AISight, the AI-Powered Precision Pathology Platform by PathAI
AISightTM is a web-based digital pathology slide viewing platform that enables the management and analysis of whole slide images.
Integrate
Cloud-native solution that is interoperable with major scanners.
Collaborate
Easy to use interface that facilitates multi-person and multi-site collaboration.
Analyze
Access to our growing algorithm menu to receive valuable insights.
AISight for Research Use
AISight can be used by biopharmaceutical companies, contract researchers, laboratories, academic institutions, and physicians to support AI-driven research.* Those researchers engaged in exploratory and clinical drug development research can leverage this platform specifically for regulated (GxP) clinical trials or translational research.
How it Works
Features
● Magnification Presets
● Slide Rotation
● Linear Measurement
● Informal Annotations with Commenting
● Viewer for Review of AI Pathologist Assist Tools
● Side-by-side Slide Viewing
● Interactive Algorithm Overlay and Heatmap Viewer
● Pen Tool to Exclude or Include Regions
● Slide Rotation
● Linear Measurement
● Informal Annotations with Commenting
● Viewer for Review of AI Pathologist Assist Tools
● Side-by-side Slide Viewing
● Interactive Algorithm Overlay and Heatmap Viewer
● Pen Tool to Exclude or Include Regions
AISight Dx
AISight Dx is our FDA 510(k) cleared digital pathology platform that can be used for the purpose of primary diagnosis in clinical settings and was validated to ensure the highest quality image resolution for clinical in-vitro diagnostic (IVD) use.+
Get In Touch with our Team
Connect with us to learn more about AISight and which version may be best suited for your work.
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*AISight is for research use only. Not for use in diagnostic procedures.
+AISight Dx is only cleared for use in primary diagnosis in the United States (U.S.) and European Union (EU). In the U.S., AISight Dx is cleared (K212361) for clinical use with the Philips Ultra Fast Scanner. In the EU, AISight Dx is CE marked for clinical use with the Philips Ultra Fast Scanner. Outside of the U.S. and EU, AISight Dx may be available for research use only or similar designation and not for use in diagnostic procedures. Contact PathAI for additional information.
+AISight Dx is only cleared for use in primary diagnosis in the United States (U.S.) and European Union (EU). In the U.S., AISight Dx is cleared (K212361) for clinical use with the Philips Ultra Fast Scanner. In the EU, AISight Dx is CE marked for clinical use with the Philips Ultra Fast Scanner. Outside of the U.S. and EU, AISight Dx may be available for research use only or similar designation and not for use in diagnostic procedures. Contact PathAI for additional information.