Patholytix

Patholytix

The Complete Regulated Ecosystem For Non-clinical Pathology

Speed up your review with the industry-leading pathology workflow, managing and interpreting your data easier and faster than ever before
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Product Description

Patholytix Is Your Single Solution For Research And Translational Pathology

Patholytix delivers a scalable, GLP compliant, digital pathology management solution including Viewer, Image QC, Storage, AI Decision support and WSI synced data capture.

Patholytix Preclinical is a fully scalable solution that grows in line with your organisational needs. Add users, expand capabilities, and add on modules to fit your use cases as you need them.

SUPERIOR ERGONOMICS IN STUDY MANAGEMENT

Patholytix is designed for physical comfort whilst you work. You are no longer hunched over a microscope. You suffer less neck and wrist strain.

Sort and review slides at the click of a button, versus 2-3 hours of tedious sorting and prep of glass slides.

Simplify your work in every single way, with no loss of detail compared to the microscope.

REVOLUTIONARY CLOUD-BASED INFRASTRUCTURE

Revolutionary cloud-based infrastructure allows on-demand collaboration between remote Pharma, CRO partners and specialist Consultants from any location around the world.

Studies can be reviewed concurrently by different pathologists, speeding up study outcomes. When combined this leads to easier and faster collaboration with partners in your network.

“Patholytix is the first viewer that adopts a study-centric approach from the ground up; combined with its excellent metadata management it makes primary evaluation, peer review and blind assessment of nonclinical toxicology studies very efficient, and in some ways even more efficient than the microscope.”

Erio Barale-Thomas
Janssen Pharmaceuticals

PATHOLOGY’S MOST FLEXIBLE STUDY TEMPLATES

Flexible study templates allow you to define your study by the parameters important to you. This data forms the information by which the study is filtered in the Study Browser. This allows you to intelligently interact with your study the way you want to – a feature not possible with any existing study management system.

ISO27001 CERTIFICATION

ISO27001 certification confirms that our entire range of services offer the confidence and security to enable the management of WSI, study metadata, and distribution of slides to partners.

Through rigorous ISO 27001 process and technical controls, your data remains secure at every point in our ecosystem – from the moment you upload a study to the point a remote partner completes their review.

HYBRID SOLUTION FOR SECURITY & PERFORMANCE

Studies are delivered to you securely ensuring data integrity, continuity and most importantly, high performance. This allows for seamless review and transition between images and resolutions.

Image viewing is identical in detail to your microscope. At the touch of a button or twist on the ergonomic mouse, you can go between magnifications very quickly and move on to the next slide.

Offering a blend of workflow design, viewing performance, and ease of use that delivers a truly unique digital pathology experience.

Additional Information

Medical Device | IVD Certifications

Product is not intended as a medical device

Clinical | Research Suitability

Research, Safety Assessment, Toxicological Pathology

Imaging Modality Supported

Brightfield

On-Premise Deployment

Hybrid cloud

Cloud Deployment

yes

Viewer Type

Scanner-agnostic, Standalone (Windows)

Z-Stacks Supported

no

TMA Support

yes

Real-time Slide Conferencing

no

Frozen Sections?

yes

DICOM Compatibility

yes, Fully native DICOM compatibility will be available late 2023. Currently DICOM exports are available from the system for archival puposes and interoperability.

File Formats Produced | Supported

.svs, Hamamatsu .ndpi, Leica .scn, Leica Aperio .ome-tif, Leica Aperio .svs, Objective Imaging .svs, Olympus .vsi, Philips .iSyntax, Philips .tiff, Roche .tif, TIFF/TIF, Ventana .bif, Zeiss .czi, .mrxs, .svslide, .vms, .vmu, Artificial Intelligence algorithms tested and validated against SVS and NDPI WSI. Quality Control algorithms tested and validated against Leica SVS and Hamamatsu NDPI WSI, Limited support may be available for Zeiss (.czi), Hamamatsu (.vms, .vmu), Zeiss (.czi), Philips (.tiff, .isyntax), Olympus (.vsi), Sakura (.svslide), Trestle (.tif)

Additional Notes*

Comprehensive content management solution for all aspects of non-clinical research., Connects Pharma and CRO both inter- and intra-organizationally to enable Primary and Peer Review of nonclinical studies., GLP compliant for both primary and peer review, allowing GLP studies to be reviewed fully digitally end to end., Offers a complete solution for study scoring, review, and management for glass and hybrid studies, as well as digital studies., Offers scoring templates for drug discovery studies such as tissue-cross reactivity (TCR), target-tissue characterization (TTC), and dose-range finding (DRF) studies., Provides a regulated ecosystem for non-clinical study and content management., Tailored solution to meet the unique needs of nonclinical safety assessment study review processes.

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