Patholytix provides a step change for the digital peer review of GLP toxicology studies. We now have a platform that puts the pathologist back in control.
Review your non-clinical studies in a digital GLP environment whilst maintaining compliance during the validation process.
Complete all your GLP work within our platform. Before Patholytix 3.0, no platform has been qualified for use in GLP primary review.
Enable or disable features such as work-from-home functionality, study archival and export, audit trail, and AI and vector annotations. Configure settings on a per-site basis to match risk assessed GLP processes and to suit regional regulatory requirements.
Deciphex can provide dedicated computer systems validation resources to help you through your validation process.
We provide advanced training for Pathologists, QA & System Admin staff to help them understand and maintain GLP-compliant utilisation of our platform.
We can now customise your GLP services package to accommodate the level of support you require. For example, you might require validation documentation but have the in-house expertise to complete the documentation. Conversely, you might have no in-house expertise and require X weekly hours support from one of our experts.
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