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Philips IntelliSite Pathology Solution Receives 510(k) Clearance

by Fred Pennic 07/12/2024 Leave a Comment

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What You Should Know: 

– Philips IntelliSite Pathology 5.1 has received 510(k) clearance from the FDA, solidifying its position as the most widely deployed digital pathology solution for primary diagnosis globally. 

– With over 300 pathology labs already implementing Philips’ solution, and over 20 labs achieving complete digital workflows, the success of this technology is evident.

Investing in the Future of Cancer Care

By empowering collaboration, boosting efficiency, and promoting accurate diagnoses, Philips IntelliSite Pathology 5.1 is a powerful tool for pathologists and ultimately improves patient outcomes in the fight against cancer.

Philips IntelliSite Pathology: The Digital Solution

Philips offers a comprehensive solution – the Philips IntelliSite Pathology Solution – to empower pathology labs with the power of digital workflows. This solution, including whole-slide scanners, an image management system, and expert implementation support, guides labs from analog to fully digital processes.

Benefits of Philips IntelliSite Pathology:

  • Enhanced Collaboration:
    • Secure remote collaboration allows pathologists to consult with colleagues for second opinions and leverage cloud-based AI applications, leading to faster and more accurate diagnoses.
    • Secure data sharing makes relevant information accessible to the entire care team, improving overall patient care coordination.
  • Improved Efficiency:
    • Digital workflows can increase pathologist efficiency by up to 21% compared to traditional methods.
    • Remote work capabilities offer flexibility and help address the ongoing shortage of pathologists.
    • Faster turnaround times for case review, reporting, and sign-off lead to quicker treatment decisions.
  • Accuracy and Precision:
    • Seamless integration of hardware, software, and analysis tools enables pathologists to deliver more accurate diagnoses.
    • Secure integration with third-party AI applications further enhances diagnostic capabilities, as demonstrated by a 27% efficiency gain and 37% productivity gain achieved using Ibex Medical Analytics’ AI software for prostate cancer detection 
  • Scalability and Openness:
    • The Philips IntelliSite Pathology Solution integrates seamlessly with existing systems and scales to meet growing demands.
    • The open-platform design facilitates the integration of future advancements, including AI-driven diagnostic tools and large-scale research initiatives.

“Digital pathology is helping to revolutionize how we diagnose and potentially treat cancer. With the 510(k) approval we expand our ability to help pathology laboratories transform to fully digital workflows, saving time and easing the burden on pathologists and patients,” said Martijn Hartjes, Clinical Informatics Business Leader at Philips. “We are advancing the digital transformation in pathology and multi-disciplinary clinical collaboration between pathologists, radiologists, oncologists, and other healthcare professionals, empowering clinicians with the tools they need to deliver improved patient outcomes and care.”

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Tagged With: FDA Clearance, FDA clearance 510k, Philips

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