Research Use Only — Not for Clinical Diagnosis

AI-Assisted Breast UltrasoundScreening Partner Program

We partner with healthcare institutions to validate AI that analyzes ultrasound images and drafts structured medical reports in seconds — as decision support, always radiologist-reviewed.

Learn How It Works
Processing Time

5–10s

Accuracy

87–92%

Sensitivity

89–94%

Partnership Cost

$0

Executive Summary

What This System Does

An AI assistant that analyzes breast ultrasound images and drafts detailed medical reports in seconds — a "second pair of eyes" that helps radiologists review images more efficiently and consistently.

Current Status

Research & Development Phase

Regulatory Status

Research Use Only

Partnership Benefit

Free System + Support

The Problem We Solve

Breast cancer is the 2nd leading cause of cancer death in women globally. Radiologists review hundreds of ultrasound images daily — time-consuming, mentally exhausting, and subject to human variability. Early detection saves lives, but the current screening process has challenges:

High Workload

Radiologists analyze hundreds of images daily, leading to fatigue and potential oversights.

Limited Access

Many regions lack specialized radiologists, causing delays in diagnosis.

Subjectivity

Inter-observer variability leads to inconsistent interpretations.

Time-Consuming

15–20 minutes per exam plus extensive report writing.

Our Solution: A 3-Stage AI Pipeline

We've developed an AI system that works like a radiologist's assistant — providing fast, consistent, and detailed analysis to support clinical decision-making.

How It Works

Every scan first passes a quality gate — poor or uninterpretable images are flagged for a re-scan rather than guessed at. From there, the pipeline runs in three stages, with the diagnosis coming from validated decision logic and the language model only writing it up:

1

Detect — “Where should I focus?”

Attention U-Net Segments the ultrasound pixel-by-pixel to locate the lesion and measure it — size, margins, shape, and location — like a radiologist outlining a suspicious area.

Output: Lesion mask plus measurable, structured features.

2

Decide — “What is this, and how sure are we?”

Vision Transformer classifier Produces a calibrated probability for each class (benign, malignant, normal) with an uncertainty estimate. Validated decision logic — not the language model — maps that probability to a BI-RADS band using a sensitivity-first threshold, and abstains to a radiologist when confidence is low.

Output: Calibrated class + provisional BI-RADS, or an explicit “low confidence → radiologist” flag.

3

Describe — “What should I document?”

GPT-5 Turns the fixed, structured findings into a professional report using proper radiological terminology. It can explain the decision, but is explicitly forbidden from changing the class or BI-RADS.

Output: Structured report with BI-RADS category and follow-up recommendations.

5–10 seconds

Total processing time per image

Example Clinical Report

AI-Generated Report (Draft)Benign · 84% confidence

LESION CHARACTERISTICS

Oval, well-circumscribed hypoechoic lesion measuring 1.2 cm. Smooth margins with parallel orientation to skin. Posterior acoustic enhancement present (suggests fluid-filled).

ANATOMICAL ASSESSMENT

Normal surrounding tissue architecture. No distortion. Skin thickness normal (2 mm).

VASCULAR FINDINGS

Normal blood flow pattern. No enlarged lymph nodes visualized.

KEY OBSERVATIONS

  • Well-circumscribed margins (benign feature)
  • Parallel orientation (benign feature)
  • No suspicious calcifications

IMPRESSION

Findings consistent with simple cyst or fibroadenoma. BI-RADS 2 (Benign). Routine screening in 12 months recommended.

The Technology

Attention U-Net

Segmentation model with attention mechanisms that focus on relevant tissue regions and measure each lesion. Trained on 3,200+ annotated images.

Vision Transformer + decision logic

A ViT classifier produces calibrated probabilities; validated rules — not the AI — set the BI-RADS band on a sensitivity-first threshold and abstain to a radiologist when unsure.

GPT-5

Language model that writes the report around the fixed decision in professional radiological terminology. It describes the findings; it never sets the diagnosis.

Performance Metrics

Overall Accuracy87–92%
Sensitivity (Malignancy Detection)89–94%
Specificity85–90%
Segmentation Quality (Dice)0.85–0.92

* Based on validation with the BUSI dataset. Real-world performance to be validated through partnership studies.

Clinical Benefits

For Radiologists

Faster Workflow

20–30% reduction in case review time, allowing focus on complex cases.

Consistent Analysis

A standardized approach reduces inter-observer variability.

Second Opinion

Independent validation catches potential oversights.

Report Templates

Pre-populated structured reports in proper BI-RADS format.

For Healthcare Facilities

Higher Throughput

Process more patients with the same resources.

Quality Assurance

Built-in quality checks and performance monitoring.

Training Tool

An educational resource for radiology residents and fellows.

Research Opportunities

Academic publications and conference presentations.

Research Partnership Program

What We're Looking For

We're seeking clinical research partners to help validate this technology in real-world settings. Together, we'll demonstrate its clinical utility and prepare for regulatory approval.

Ideal Partner Profile

  • Hospital, clinic, or imaging center with breast ultrasound capabilities
  • Access to a diverse patient population
  • Interest in AI-assisted diagnostics research
  • Institutional ethics committee for research approval

What You'll Receive

  • Free complete AI system during the research phase
  • Free installation, training & technical support
  • Co-authorship on research publications
  • Early access to the commercial version

Partnership Timeline

Phase 1: Pilot Study

Months 1–3
  • System installation at your facility
  • Staff training (radiologists & technologists)
  • Process first 50–100 cases
  • Collect initial feedback and identify technical issues

Phase 2: Validation Study

Months 4–9
  • Process 300–500 patient cases
  • Compare AI vs. radiologist readings
  • Measure sensitivity, specificity, and agreement rates
  • Document edge cases and refine the AI

Phase 3: Clinical Integration

Months 10–12
  • Integrate into daily clinical workflow
  • Monitor efficiency improvements and time savings
  • Assess user satisfaction
  • Prepare a co-authored publication

Time Commitment

Initial Setup

1–2 days for installation & training

Weekly Reviews

1–2 hours per week for case review

Monthly Meetings

1 hour for progress updates

Safety & Regulatory Status

Critical Safety Information

This AI is not a substitute for radiologist interpretation. It serves as a clinical decision-support tool only.

What the AI can do

  • Assist in identifying regions of interest
  • Provide preliminary classification
  • Generate report templates
  • Serve as a second opinion

What the AI cannot do

  • Replace clinical judgment
  • Make final diagnostic decisions
  • Account for clinical history
  • Consider patient symptoms

Regulatory Status

Current Status

Research & Development Phase

Approved Use

Research with institutional approval

Approved for: research studies with institutional approval, educational purposes, and clinical decision support with radiologist verification.

Frequently Asked Questions

Limited partnership slots available

Ready to pioneer AI in breast cancer screening?

Join healthcare institutions validating this technology. Be among the first to access the system at no cost during the research phase.

Zero Cost

Free system, installation & support

Co-Authorship

Publications & academic recognition

Early Access

Priority for the commercial version

Your data stays secure. Compliant with local regulations. Ethics committee support provided.

Get Started

Contact Information

Response Time

We typically respond to partnership inquiries within 24 hours. Our team is glad to discuss how we can collaborate with your institution.

Quick Partnership Request

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No commitment required to schedule a call
Free consultation on partnership opportunities
Custom study design for your facility

Important Disclaimer

Research Use Only: This AI system is currently under development and validation. It is not approved for standalone clinical diagnosis.

Clinical Responsibility: The interpreting radiologist retains full responsibility for all diagnostic decisions. AI outputs are advisory only.

No Warranties: While we strive for accuracy, AI systems can make errors. Always verify AI findings independently.

Data Privacy: We comply with all applicable data protection regulations. Specific protections are detailed in partnership agreements.