Digital PathologySolutions

AI biomarker scoring, built for routine practice.

Clinical workflow software that supports biomarker measurement and review, with final interpretation remaining with the reporting professional.

Ki-67 IHC stain
HER2 IHC stain
ER IHC stain
PR IHC stain
PD-L1 IHC stain
TRBC1 / CD3 IHC stain
CD4 / CD8 IHC stain
p53 IHC stain

Recognition Built on Clinical Reality

Our clinical page describes software workflows and product information. Intended use, evaluation, and regulatory status depend on the relevant product documentation and jurisdiction.

Product information mark

Clinical workflow modules

HER2 Analysis

Standardized Breast Diagnostics

Breast Suite

An AI-assisted suite for breast biomarker review — HER2, Ki-67, ER, and PR — with configured scoring workflows subject to the relevant documentation.

PD-L1 Analysis

Immuno-Oncology Diagnostics

Immuno-Oncology Suite

Cell-type and quantitative review fields for PD-L1, p53, CD4/CD8, and TRBC1/CD3 workflows, subject to the relevant documentation.

Elevate your clinical workflow

Whether you are reviewing a single AI module or planning a digital pathology environment, the workflow can be scoped around documentation, local evaluation, and specialist review.

From slide ingest through review, the workflow can be documented and evaluated against the laboratory's requirements. Interfaces and reporting steps depend on the product configuration.

Workflow review

One documented path

  • Slide ingest

    WSI · 40× scan

    01
  • AI analysis

    Region segmentation

    02
  • Review field

    Biomarker readout

    03
  • Report review

    Configured report field

    04

What labs gain from AI-assisted reporting

Documented workflows, specialist review, and project-specific evaluation.

  • Faster turnaround times

    Reduce case processing from hours to minutes.

  • Reproducible results

    AI consistency removes observer variability.

  • Secure digital workflow

    Protected slide sharing, remote access and streamlined collaboration.

FAQ

Deployment, validation, and how the modules fit into your existing workflow.

Modules can provide review support inside a configured workflow. Inputs, interfaces, outputs, and the final professional decision depend on the relevant product documentation and service scope.

Deployment can be phased through assessment, design, testing, and supervised evaluation, according to the host institution's data-governance and workflow requirements. Available environments depend on the service scope.

Available modules and biomarkers depend on the product documentation and intended use. Research workflows and custom model evaluation are scoped through the research platform.

Product status and evaluation requirements depend on the relevant documentation and jurisdiction. Local testing may be included in a project before routine use.

Still wondering?

Don't waste time in uncertainty.

Our team is ready to walk through implementation details.

Get in touch

Speak with our pathology team

Tell us about your laboratory, the case mix you work with, and the workflow you want to evolve. We will tailor the demonstration and validation plan to match your exact protocols, scanners, and reporting habits.

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