Digital pathology
Digitize your pathology workflow with fast, high-quality scanning capabilities
Accelerate the path from images to answers
Philips is your experienced partner in your digital transformation journey and offers the tools and resources for every stage of the pathology process. With a comprehensive, and end-to-end experience we help to empower pathologists to improve efficiency, diagnostic confidence and collaboration.
With our pathology slide scanners, the Image Management System (IMS) and a comprehensive set of software tools and capabilities, you can easily connect with supporting sub-specialists around the world on the quest for quick and confident diagnostic decisions that enhance patient care.
Featured products in Digital pathology
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Pathology Scanner SG20
SG20 is designed to accommodate laboratories with low volume spoke labs (within a network) or small independent labs. With a high first time right, medium throughput and load and walk away scanning, the SG20 enables you to digitize your histology samples and obtain high quality clinical diagnostic images for routine use and integrated pathology networks.
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Pathology Scanner SG60
SG60 is designed to accommodate laboratories with a lean workflow and need to scan small batches of slides to achieve operational excellence and short turnaround times by scanning batches in parallel. With a high first time right, high throughput, load and walk away scanning, the SG60 enables you to digitize your histology samples and obtain high quality clinical diagnostic images for routine use and integrated pathology networks.
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Pathology Scanner SG300
SG300 is designed to accommodate laboratories for high volume labs that want to maximize scanner utilization and further reduce the total cost of ownership per slide by means of overnight scanning. With its high first time right, high throughput and load and walk away scanning, the SG300 enables you to digitize your histology samples and obtain high quality clinical diagnostic images for routine use and integrated pathology networks.
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High-quality digitization that truly enables digital pathology networks
With our digital pathology solution** you can digitize your workflow with consistently high image quality and fast first-time-right scanning capabilities. Maximize diagnostic confidence and high throughput with a first-time-right rate of 99.5%*, enabling laboratory efficiency and fast turnarounds, thanks to a new scanner platform with a range of high-performing digital scanner models.
Gain new insights through real-time collaboration
IntelliSite Image Management System features software and algorithms designed to aid your efficiency, streamline workflow and maximize diagnostic confidence. This enhances the user experience by combining fast and easy digital workflow with smart case load management to allow for real-time collaboration and case sharing for improved patient care.*
Unify patient data in a streamlined workflow with bidirectional LIS integration
An updated case viewer enables multi-disciplinary patient data review and care pathway selection.
Connect your teams with a scalable solution with easy sharing of patient-centric histology data
Share across organizations and among sites through an open solution that enables enhanced interoperability options. Share across organizations and among sites through an open solution that enables enhanced interoperability options.
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Footnotes
*Survey of 52 pathologists, lab managers and lab technicians in Europe, 2018. Results are specific to the institution where they were obtained and may not reflect the results achievable at other institutions. **The digital pathology solution is a bundle of: Pathology Scanner Second Generation SG20/ SG60/ SG300 • Image Management System Viewer • Image Management System Application Server and Storage Software • High quality 27” monitor validated with the IVD solution (US only) Under the EUA ,the use of PIPS in the USA was allowed and now with the end of the EUA ,Philips Is pursuing a 510k clearance for the PIPS device. Philips IntelliSite Pathology Solution is in conformance with Regulation (EU) 201 7/746 of the European Parliament and of the Council of 5 April 2017 on In Vitro Diagnostics (IVDR).
