Global R&D Strategy · Product Pipeline
Innovation Pipeline.0-to-1 at Scale.
A portfolio of breakthrough healthcare technologies spanning diagnostics, AI-enabled systems, connected medical devices and FDA-focused innovations — from early research through commercialization.
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Innovation Programs
NIH
Research Funding
FDA
Regulatory Strategy
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Product Development
Featured Programs
Explore the
Innovation Portfolio
Every program represents a distinct stage of research, engineering, clinical validation and commercial readiness.
EMRAST
Early Multi-Modal Alzheimer's Risk Assessment & Sensing Technology
$2.95M · R44AG082621
Multimodal diagnostic platform combining psychophysical olfactory stimulation with ML-based biomarker classification for pre-clinical Alzheimer's detection. Randomized feasibility trial published in Alzheimer's & Dementia.
EDITOR
Early Detection & Intervention Tool for Opioid Recovery
$2.70M · R44DA056156
Connected RPM ecosystem with a novel non-infrared pupillometer enabling objective neurological assessment for opioid use disorder monitoring and MAT efficacy evaluation.
CBOT-P
Chronic Pain Neurosensory Therapeutic Platform
$2.79M · R44AG061981
FDA Breakthrough Device designated electromechanical neurostimulation platform for chronic pain. ISO 13485 QMS compliant. Real-time neural feedback with electromechanical precision actuation.
MemoryDriver
AI-Powered Digital Therapeutic for Cognitive Longevity
Commercial
Patented iOS digital therapeutic combining AI-driven cognitive assessments with personalized brain training. HIPAA-compliant, AWS-hosted, with longitudinal performance tracking — built 0-to-1 as a commercial product.
Smart Nasal Cannula
Connected Respiratory Monitoring Platform
R&D
BLE 5.0 + AWS IoT Core connected wearable with 0.1 L/min micro-flow sensing, SpO₂, PPG, and edge AI for 48+ hour remote respiratory monitoring.
COT
Cognitive Optimization Therapy — Disease-Modifying Alzheimer's Intervention
$3.13M · R44NS125745
End-to-end hardware lifecycle for an Alzheimer's disease-modifying intervention device with full ISO 13485 / IEC 62304 compliance and usability engineering per IEC 62366.
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Whether you're funding translational research, navigating an FDA pathway, or scaling a device program from bench to market — let's talk.