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.
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 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.
Complete your study reviews from home or in the office. Save time travelling and shipping slides.
You have complete control over the structure of your studies, supporting any type of associated data, study size, and WSI vendor format - including SEND data representation and LIMS integration capabilities - within a simple, intuitive interface.
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.
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.
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.
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.
SPEED UP YOUR REVIEWS AND DRUG DEVELOPMENT TIME
REVIEW & SCORE DRUG DISCOVERY STUDIES DIGITALLY FOR THE FIRST TIME
ACHIEVE IMAGE QUALITY AT SPEEDS BEYOND HUMAN CAPABILITIES
REACH CRITICAL DECISIONS FASTER, AND WITH GREATER CONFIDENCE
END-TO-END GLP-COMPLIANT DIGITAL STUDIES (A WORLD FIRST)
UNLOCK HISTORICAL PATHOLOGY KNOWLEDGE