Your Technical Quarterback for Longevity & Health Robotics

Technical Due Diligence for Longevity & Health Robotics Investments

I assemble the right technical and regulatory experts to de-risk your investments. Your technical quarterback for FDA pathways, HIPAA compliance, and health-tech architecture—bringing in specialists when you need them most.

FDA/510(k) Experience
HIPAA-Compliant Architecture
Curated Expert Network

Who I Work With

Specialized technical advisory for the longevity and health robotics ecosystem

VCs & Angels

I assemble technical assessment teams for longevity biotech and health robotics investments. You get comprehensive due diligence without managing multiple vendors—I coordinate the right specialists and synthesize their findings.

Founders & CTOs

I connect you with the right experts for FDA submissions, security audits, and clinical validation. Think of me as your technical quarterback who knows exactly who to bring in and when.

Technical Leaders

Get strategic guidance plus access to my curated network of regulatory consultants, security experts, and clinical specialists. Fractional CTO services with a full bench of domain experts behind me.

How I Work

Your technical quarterback who orchestrates expert teams

I Don't Pretend to Know Everything—And That's the Point

The longevity and health robotics space is too complex for any one person to be the expert in everything. FDA regulatory strategy, cybersecurity compliance, clinical validation, materials science—each requires deep domain expertise.

My value is knowing exactly which specialists to bring in and when. I've built relationships with top-tier regulatory consultants, security auditors, clinical researchers, and domain experts. When you work with me, you get:

  • One point of contact instead of managing multiple vendors
  • Pre-vetted specialists who I've worked with on similar projects
  • Coordinated deliverables that actually answer your questions
  • Honest guidance—if I don't know something, I'll tell you and find someone who does

FDA & Regulatory Strategy

Consultants who've guided 50+ medical device submissions through 510(k), De Novo, and PMA pathways.

Clinical Validation & QA

Clinical specialists and QA professionals experienced in digital health studies and medical device testing.

Cybersecurity & Compliance

Security auditors specializing in HIPAA, medical device security (FDA premarket), and health data protection.

Domain Experts

PhDs and MDs in longevity research, geriatrics, materials science, and health robotics for specialized technical questions.

Consulting Services

Flexible tiers to match your needs and budget—scale up specialist support as complexity demands

Technical Due Diligence

VCs and angels evaluating longevity biotech, elder care robotics, or digital health investments at any stage.

Foundation
$40K–$55K
1–2 weeks

Core technical assessment for straightforward investments

Architecture & scalability deep-dive
Technical debt and code quality review
Team capability assessment
IP evaluation and competitive analysis
Risk-prioritized remediation roadmap
Executive summary with go/no-go recommendation
Most Popular
Standard
$70K–$100K
2–3 weeks

Foundation + one specialist for regulated products

Everything in Foundation
Regulatory compliance assessment (FDA, HIPAA, or GxP)
OR Security audit and penetration testing
Specialist expert report with findings
Integrated risk assessment across technical + regulatory/security
Comprehensive
$120K–$175K
3–4 weeks

Full specialist team for high-stakes investments

Everything in Standard
Multi-specialist coordination (regulatory + security + clinical)
Deep regulatory pathway analysis (510(k)/De Novo strategy)
Clinical validation requirements assessment
Security & compliance architecture review
Comprehensive go-to-market technical risk report

Regulatory & AI Readiness

Health-tech startups preparing for 510(k), De Novo, or clinical validation who need a clear path to regulatory approval.

Gap Analysis
$25K–$35K
1–2 weeks

Identify what's needed for FDA submission

Gap analysis vs. FDA AI/ML guidance
Data architecture review (lineage, provenance)
Model governance framework assessment
90-day implementation roadmap
Resource and cost estimates
Most Popular
Implementation Ready
$50K–$75K
2–3 weeks

Gap Analysis + regulatory consultant for execution plan

Everything in Gap Analysis
FDA regulatory consultant assessment
Validation protocol templates (IQ/OQ/PQ)
HIPAA/GxP compliance architecture design
Risk management file (ISO 14971) framework
Detailed submission preparation checklist
Submission Ready
$90K–$130K
3–4 weeks

Full team to get submission-ready documentation

Everything in Implementation Ready
Security architecture review and testing
Clinical validation strategy with MD/clinical consultant
Complete data lifecycle documentation
Audit trail and change control implementation
Submission-ready technical documentation package

Fractional Engineering Leadership

Seed to Series A longevity/health-tech startups needing strategic technical leadership without a full-time CTO commitment.

Advisory
$10K/mo
1 day/week

Strategic technical guidance for key decisions

Weekly strategic architecture decisions
Build vs. buy analysis
Technical roadmap planning
Investor relations support (technical narratives)
Monthly written updates and recommendations
Most Popular
Engaged
$16K/mo
2 days/week

Hands-on technical leadership and team building

Everything in Advisory
Hands-on architecture and code review
Technical hiring and team scaling
Regulatory compliance planning (with specialist support)
Direct Slack/email access for urgent decisions
Quarterly board presentation support

Note: Specialist consultations (regulatory, security, clinical) available at $3K–$5K per engagement as needed.

Need Something Custom?

Every situation is unique. I'll assemble the right specialist team for your specific technical, regulatory, or clinical needs. Large acquisitions, complex regulatory pathways, or novel technologies often require custom engagements.

Discuss your specific needs

Technical Expertise

Hands-on experience building longevity and health robotics systems

These case studies demonstrate my hands-on technical expertise in medical device architecture, FDA regulatory pathways, HIPAA-compliant systems, and edge AI for healthcare. This depth of knowledge—combined with my expert network—ensures comprehensive assessments and actionable recommendations.

OrbCare — Autonomous Health Monitoring Robot case study illustration
Medical DevicesRoboticsFDA Design ControlsEdge AI

OrbCare — Autonomous Health Monitoring Robot

Medical device architecture for autonomous elder care robot with 12+ vital sensors, fall detection, and edge AI. Demonstrates deep expertise in embedded medical systems, FDA design controls, and edge computing for healthcare.

Vital Sensors
12+
Response Time
< 2s
Lumi — AI Health Concierge for Chronic Care case study illustration
Conversational AIHIPAA ComplianceDigital HealthClinical Validation

Lumi — AI Health Concierge for Chronic Care

HIPAA-compliant conversational AI platform for chronic condition management and medication adherence. Experience with clinical validation strategies, multi-modal health data integration, and care coordination systems.

Context Memory
10K msgs
Adherence Lift
+47%
Nanotech AI — Longevity Materials Discovery case study illustration
ML InfrastructureMaterials ScienceLongevity BiotechResearch Platforms

Nanotech AI — Longevity Materials Discovery

ML platform for discovering biocompatible nanomaterials for life extension applications. Research-grade ML infrastructure, materials informatics, and longevity biotech product development experience.

Model Accuracy
94.2%
Candidates
5K+
Multimodal Biomarker Analysis Platform case study illustration
Data IntegrationFHIR/HL7Predictive AnalyticsHealth Platforms

Multimodal Biomarker Analysis Platform

Health data integration platform combining wearables, labs, and genetic data for predictive longevity insights. FHIR/HL7 standards expertise, regulatory-grade data pipelines, and real-time health analytics.

Data Sources
25+
Processing
Real-time

Why This Approach Works

The advantages of working with a technical orchestrator

For Investors

  • One comprehensive assessment instead of managing multiple consultants
  • Pre-vetted specialists who know the longevity/health robotics space
  • Synthesized findings with clear go/no-go recommendations
  • Flexible pricing—pay for the tier of expertise you actually need

For Founders

  • Start with Foundation tier, scale up as complexity grows
  • Access to top regulatory and clinical experts without the search
  • Coordinated guidance from technical + regulatory + clinical perspectives
  • Transparent about what I know vs. when to bring in experts

Mission-Aligned

I'm deeply committed to extending healthspan and improving elder care through technology. This isn't just consulting—it's advancing a mission I'm personally invested in through my own longevity health-tech products. When I bring in specialists, they share this commitment.

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