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PathAI vs Paige AI

This comparison was retrieved by database IDs selected from the catalog.

PathAI favicon

PathAI

PathAI

Paige AI favicon

Paige AI

Paige

Overview
Rating
—
—
Category
Developer Tools
Developer Tools
Subcategory
AI Pathology Diagnostics
AI Oncology Pathology
Company
PathAI
Paige
Status
Active
Active
Launch year
2019
2021
Tags
pathologyaicancerdiagnosticsimagingpharmaceutical
pathologyaicanceroncologyfdadiagnostics
Pricing
Starting price
FreeBest value
Free
Pricing model
Enterprise
Enterprise
Free plan
No
No
Free trial
✕
✕
Pricing notes

Enterprise and pharmaceutical partner licensing. No public pricing or individual access.

Enterprise licensing to health systems and pathology labs. No public pricing or individual access.

Capabilities
Best for
AI-assisted cancer pathology diagnosisClinical trial patient selectionDrug development biomarker discoveryPathology lab productivityCompanion diagnostic development
AI-assisted prostate cancer pathologyFDA-cleared clinical AI pathologyOncology pathology quality assuranceDigital pathology AI adoptionCancer detection sensitivity improvement
Target audience
PathologistsOncology clinical trial teamsPharmaceutical R&DAnatomic pathology labsHospital pathology departments
PathologistsAnatomic pathology lab directorsHospital pathology departmentsOncology clinical teamsDigital pathology adoption leaders
AI type
Computer Vision
Computer Vision
Modalities
ImageData
ImageData
Technical
Model provider
PathAI
Paige
Model names
—
—
API available
✕
✕
Open source
✕
✕
Deployment
EnterpriseSaaS
EnterpriseSaaS
Platforms
WebLIS integrated
WebLIS integrated
Integrations
EpicCernerAperioHamamatsuAPI
AperioHamamatsuPhilipsEpicAPI
Team collaboration
✕
✕
Trust & security
Security

HIPAA compliant with BAA. ISO 13485. FDA clearance for specific indications. Enterprise data handling agreements.

HIPAA compliant with BAA. FDA De Novo authorisation (Paige Prostate). ISO 13485 medical device quality management. Enterprise data handling agreements.

Privacy notes

Digital pathology slide data processed under HIPAA BAA. FDA clearance for clinical use is indication-specific — review regulatory status for each intended use.

Digital pathology slide data processed under HIPAA BAA with medical device security standards. FDA authorised for specific clinical indications.

Verdict
Pros
  • Demonstrable accuracy in specific cancer diagnosis tasks on large pathology slide datasets
  • Pharmaceutical partner programme with BMS, AstraZeneca, and Gilead validates clinical credibility
  • Consistent quantification across large sample sets improves on inter-pathologist variability
  • FDA-cleared tools for specific clinical indications
  • First FDA De Novo authorisation for AI clinical pathology — critical regulatory differentiator for clinical deployment
  • Published clinical evidence shows improved cancer detection with AI-assisted pathologists
  • Expanding cancer type coverage builds on the regulatory foundation for prostate cancer
  • Academic medical centre partnerships provide credible clinical reference implementations
Cons
  • Enterprise and pharmaceutical partner model — not accessible to individual pathology labs
  • Regulatory clearance is indication-specific — clinical use requires FDA-cleared indications only
  • ROI case requires high-volume pathology operation or significant clinical trial programme
  • Enterprise licensing only — not accessible to individual pathologists or small labs
  • FDA authorisation is indication-specific — Paige Prostate is cleared; other cancer types are in different regulatory stages
  • Clinical AI pathology adoption requires significant workflow integration and pathologist training investment

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