Be the First to Shape AI in Oncology

Pilot Program

Who the Pilot Is For

Hospitals and imaging/pathology centres evaluating AI decision support with clear clinical and operational goals.

Outcomes We Target

• Verified model performance on your data

• Safe, reversible integration into your workflow

• Economic case (time-to-report, second-read uplift, avoided recalls)

• Clear go/no-go criteria for production

Pilot Timeline (Typical)

• Week 0–1 : Readiness & Governance
  • NDA/DPA/IMA executed • Data sharing plan • IT & privacy approvals • Success metrics finalized

• Week 1–2 : Integration
  • Connector/agent install • DICOMweb/WSI pipeline setup • SSO & RBAC • Test round-trip

• Week 2–3 : Validation on Local Data
  • Site-specific threshold tuning (pre-specified) • Performance analysis • Bias checks

• Week 3–4 : Workflow Trial
  • Reader-in-the-loop • Safety guardrails • Feedback capture • TAT/time savings study

• (Optional) Week 5–6 : Extended Evaluation
  • Additional indications • IT hardening • Procurement package preparation

Success Metrics (Examples)

• AUROC ≥ X; Sensitivity at Spec Y ≥ target

• Triage uplift ≥ N% on priority cases

• Time-to-report reduced by ≥ M minutes

• Zero critical incidents; audit log completeness = 100%

Roles & Responsibilities

Customer: Data governance approval, IT coordination, clinical SME time, success metric sign-off.
PrediX: Integration, configuration, training, monitoring dashboards, validation report.

Data Requirements

• Radiology: DICOM MRI sequences as defined in pilot SOW

• Pathology: WSI (SVS/NDPI/OME-TIFF, etc.) with slide-level labels

• De-identified where required; transfer via secure channel

IT Requirements

• Network egress to Canadian cloud endpoints or on-prem compute

• SSO integration (SAML/OIDC); service account for PACS/LIS where needed

Deliverables

• Pilot Validation Report (metrics + CI, by indication)

• Safety & Risk Assessment

• Integration Runbook

• Executive Summary & ROI model

Consent & regulatory

By requesting a pilot you acknowledge that PrediX is investigational and not for primary diagnosis unless and until licensed.

Start a Pilot
Email PrediX-Pilot@Finosoft.ca with your site profile and target indications.

Request a Trial

What you get in 4–6 weeks

• Integration with your PACS/LIS or pathology systems

• Validation on your data with agreed metrics and confidence intervals

• Safety guardrails and reader-in-the-loop workflow

• Executive summary with ROI and go/no‑go recommendation

What we need from you
Site profile, target indications, IT/Privacy contact, and a small evaluation dataset .

Request form (fields to include)
Name · Role · Institution · Email · Phone · Modality (MRI/WSI) · Indication(s) · Viewer/PACS/LIS · Cloud/On‑prem · Target timeline · Notes

SLA
We aim to respond within 2 business days with next steps.

Consent & regulatory
By requesting a pilot you acknowledge that Predix is investigational and not for primary diagnosis unless and until licensed.

Trial or Pilot Request

Simply send your request, That's all.....