Live Platform

Turn Every Lab Result into a
24/7 Digital Clinic

Increase repeat testing and patient-driven downstream revenue without changing your LIS or taking on clinical risk.

No IT integration required
No change to clinical liability
HIPAA & GDPR aligned by design
Web app live
Mobile app April 2026
The Business Case

Why This Matters to Your P&L

Regain is not a value-add. It is a revenue multiplier.

repeat testing
vs 1.2x baseline
Measured on an annualized per-patient basis
+10%
net new revenue
from patient execution (care, services, follow-ups)
$0
incremental cost
operational overhead

Observed in early partner cohorts under real-world operating conditions. Conservative targets shown.

Relative to matched patients receiving standard PDF-based reporting.

Why Patients Come Back

Before

Static PDF report

No guidance, no follow-up

Patient confusion

One test per year

After

Daily protocol tied to biomarkers

Clear, actionable plans

Progress requires verification

Four tests per year

Diagnostics become an ongoing relationship, not a one-time event.

Patients return because measurable improvement requires objective verification through clinically appropriate follow-up testing.

The Retesting Flywheel

How Regain Multiplies Test Volume

The Problem

Patients don't re-test because they don't know what to change.

What Regain Does

1

Explains why a marker is off

Clear, mechanism-first explanations patients can understand

2

Guides daily lifestyle actions

Diet, sleep, activity protocols tied to their specific biomarkers

3

Frames improvement as a measurable hypothesis tied to specific biomarkers

Patients want to verify their progress through follow-up labs

Verification occurs through clinically appropriate follow-up laboratory testing.

Follow-up intervals are aligned with established clinical guidelines and standard practice.

The Result

Patients optimizing their health need follow-up labs to verify progress.

"Optimization without measurement is guesswork. Regain turns improvement into a reason to re-test."
Risk Mitigation

The Two-Zone Safety Shield

Clinical liability remains exactly where it is today.

Zone 1

Clinical Zone

Owner You
Function Official diagnostic reporting
Liability Unchanged
What's Included
Your validated PDF report
Your reference ranges and flags
Your branding and signatures
Medical-grade accuracy
Zone 2

Lifestyle Zone

Owner Regain
Function Daily coaching and execution
Liability Regain
What's Included
Lifestyle optimization protocols
Nutrition, sleep, activity guidance
Non-diagnostic, non-prescriptive coaching

The zones are cryptographically and contractually isolated. The lines never cross.

Regain does not infer diagnoses, change reference ranges, alter clinical conclusions, or modify, suppress, or prioritize clinical findings.

Regain does not order, schedule, or mandate laboratory tests.

The Platform

A Care Team in the Patient's Pocket

Regain supports continuous patient engagement between clinically appropriate testing events.

Current
Web app
AI explanations
Personalized insights
Lifestyle protocols
April 2026
Mobile app
Wearable sync
Photo meal logging
Real-time coaching
Learn more about Regain Health

Care Roles

Nutrition

metabolic optimization

Sleep

recovery & HRV

Movement

cardiovascular & longevity

Stress

adherence & behavior change

LifeSense

Regain LifeSense: From Biomarker to Insight, from Insight to Action

The Problem

Labs lose value when patients don't act.

LifeSense is Regain's execution layer. It allows patients to act on verified lab abnormalities without leaving your ecosystem.

How It Works

LifeSense cannot activate without a validated lab result

Activates only when a lab marker is abnormal.

Recommendations must map to a biological mechanism

Fully embedded in the lab explanation flow

No browsing, no search, no feed

What It Will Never Do

No banners or display placement
No sponsored placements
No pay-to-rank
No influence on clinical interpretation

LifeSense is not an advertising platform. It only exists when real lab data creates a real health need.

Recommendation logic is identical with or without monetization.

If a lab abnormality resolves, the corresponding execution pathway is removed.

Economics

Aligned Economics. No Hidden Fees.

How It Works

1

LifeSense adds a small execution fee to relevant services

The execution fee covers scheduling, secure data transfer, consent handling, and follow-up tracking.

Fees are not tied to referral volume, provider selection, or clinical decision-making.

Fees are fixed, transparent, and independent of clinical outcomes or provider choice.

2

Fee is shared with the lab

3

Revenue only exists if the patient acts

Revenue Split

Lab 50%
Your Share
Regain 50%
Regain Share

If recommendations don't work, engagement drops. Bad recommendations lose money.

For Medical Centers

The Highest-Intent Clinical Moment

The moment a patient sees an abnormal result is the highest-intent moment in healthcare.

LifeSense allows your own services to be offered as an optional next step when the need is revealed.

Example
LDL Cholesterol
160 mg/dL
Cardiovascular risk identified

No billboards. No wasted spend. Only relevant action at the moment of truth.

Patients may also choose to take no action or consult their existing provider.

AI Differentiation

Glass Box AI, Not Black Box Guessing

?
Others

Black Box

Opaque scores
Probabilistic fear
"80% chance of X"
Regain

Glass Box

Explanatory reasoning
Mechanism-first logic
Actionable verifiable steps
Transparent science

Explanations are citable, inspectable, and tied to measurable biomarkers.

If biomarkers do not change as predicted, the explanation is revisited or withdrawn.

All explanation logic is subject to continuous review and update as evidence evolves.

Escalation pathways defer to licensed clinicians where clinical judgment is required.

"Patients trust what they understand. Trust drives daily use. Daily use drives re-testing."

Frequently Asked Questions

Direct answers to your most critical concerns

For Lab CEOs

No.

LifeSense does not sell attention. It only activates after a verified lab abnormality and only surfaces mechanistically relevant execution options. No lab signal, no recommendations.

Yes. We go far beyond basic compliance.

Our platform operates on a 'Zero-Resident PHI' principle, providing a cryptographically enforced safe harbor for HIPAA and GDPR compliance. We secure every clinical document with non-exportable Transit keys and unique per-document encryption, ensuring raw files are purged immediately after processing. This architecture shields your institution from liability by pinning all AI processing and storage to your specific jurisdiction via a 'fail-closed' routing gateway. We provide a transparent, SHA-256 hashed audit trail, ensuring that your institutional compliance is provable, automated, and mathematically absolute.

We solved this with our 'Glass Box' engine.

Unlike 'Black Box' AI that guesses, our engine uses Explanatory Reasoning grounded in the American College of Lifestyle Medicine (ACLM) pillars.

  • No 'Wellness Woo-Woo': All protocols are based on clinical guidelines (e.g., 'Walk 15 mins after meals to blunt glucose spike').
  • Traceability: Every recommendation cites its source.
  • Liability Shield: Our 'Zone 2' architecture places the liability for lifestyle coaching on us, not you. Your brand remains associated with the clinical truth (the lab results).

Today, there's nothing to download. Our web app works instantly in any browser.

The patient experience is seamless:

  1. Tap: Patient taps the secure link (via SMS, WhatsApp, Telegram, etc.).
  2. Open: The web app loads instantly—no download required.
  3. Magic: The platform automatically logs them in and opens directly to their report.
  • No Account Creation: We pre-populate their profile using the data from the lab report.
  • No Typing: They don't need to type their name, DOB, or create a password to see their first result.
  • Result: Zero download friction means drastically higher conversion rates from 'Link Click' to 'Active User.'

Coming April 2026: Our mobile app will use 'Magic Links' for seamless app store → auto-login → direct-to-report experiences for patients who prefer native apps.

Because execution has real cost.

LifeSense charges a transparent platform fee for operating the execution layer: scheduling, consent handling, secure data transfer, audit logging, and follow-up tracking.

The recommendation exists regardless of payment. The fee does not influence what is shown, only how execution is facilitated.

No LIS changes required. Integration is minimal.

We work with your existing report output—typically PDF or HL7 via secure API or SFTP. No changes to your laboratory information system, workflows, or staff training. Reports flow through existing channels; we add the patient-facing layer on top.

Never. Your data stays in your ecosystem.

Each laboratory operates in a cryptographically isolated environment. Your patient data, operational metrics, and business intelligence are never shared, aggregated, or visible to other laboratories. We are your partner, not your competitor's data source.

Your operations continue unaffected.

Regain is an add-on layer, not a dependency. If we cease operations, your laboratory returns to baseline PDF delivery. No patient data is held hostage—you retain full export rights. We are designed to be valuable, not indispensable infrastructure.

Yes, with documented methodology.

The 4× figure is measured on an annualized per-patient basis, observed in early partner cohorts under real-world operating conditions, relative to matched patients receiving standard PDF-based reporting. Baseline industry average is approximately 1.2 tests per patient per year. Conservative targets are shown. We can provide full methodology documentation upon request.

For Regulators & Compliance

No. Our fee structure is designed to avoid AKS exposure.

Platform fees are fixed, transparent, and independent of referral volume, provider selection, or clinical outcomes. There is no per-referral payment, no volume incentive, and no pay-to-rank. The fee covers execution infrastructure, not patient steering.

No. Regain is not a medical device and does not require FDA clearance.

We do not diagnose, treat, or prescribe. Regain explains laboratory results and supports lifestyle execution based on established clinical guidelines. Clinical interpretation, diagnosis, and medical decision-making remain the exclusive responsibility of the laboratory and licensed providers.

No. Patient choice is preserved at every step.

All execution options are patient-initiated and optional. Patients may choose to take no action, consult their existing provider, or use their own resources. LifeSense surfaces mechanistically relevant options—it does not mandate, prioritize, or incentivize any specific provider selection.

Absolutely not.

Regain does not infer diagnoses, change reference ranges, alter clinical conclusions, or modify, suppress, or prioritize clinical findings. The laboratory's clinical interpretation remains unchanged and authoritative. Zone 1 (the clinical layer) belongs entirely to the lab.

The laboratory retains data ownership. We cannot and will not sell patient data.

Regain acts as a data processor under GDPR/HIPAA. Processing is strictly limited to report explanation, lifestyle execution, and patient-requested actions. We do not aggregate, resell, or monetize patient data in any form.

Lifestyle recommendations carry Regain's liability, not the laboratory's.

Our Two-Zone architecture separates clinical truth (laboratory domain) from lifestyle execution (Regain domain). Zone 1 clinical interpretation liability stays with the laboratory. Zone 2 lifestyle recommendation liability stays with Regain. The laboratory brand remains associated only with the lab results produced.

No. Retesting is driven by clinical need, not incentive.

Regain does not order, schedule, or mandate laboratory tests. Follow-up intervals are aligned with established clinical guidelines and standard practice. Patients choose whether to verify improvement through follow-up testing—Regain simply creates the conditions where verification has meaning.

We built falsifiability into the system.

Explanations are citable, inspectable, and tied to measurable biomarkers. If biomarkers do not change as predicted, the explanation is revisited or withdrawn. All explanation logic is subject to continuous review and update as evidence evolves. Escalation pathways defer to licensed clinicians where clinical judgment is required.

Consent is explicit, granular, and revocable.

Patients consent to receive explanations and lifestyle support when they access their report. Each subsequent action (scheduling, data sharing, execution) requires additional explicit consent. Patients can revoke consent and delete their data at any time.

We provide full audit documentation.

Every transaction, consent event, and data access is logged with SHA-256 hashed audit trails. We can produce complete regulatory documentation on demand: data processing agreements, consent records, fee structures, and compliance certifications. You will never be surprised by a question you cannot answer.

No. Regain is not intended for emergency or acute care use.

Regain supports lifestyle execution and long-term health optimization based on routine laboratory testing. Critical values, acute conditions, and emergency situations require immediate clinical intervention through established medical channels—not a lifestyle app.

Still have questions? Contact me directly:

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Request Data Pilot

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50% discount for 24 months
Direct influence on product roadmap
Priority support

Regain supports lifestyle execution and tracking. Clinical interpretation, diagnosis, and medical decision-making remain the responsibility of the laboratory and licensed providers. Regain is not intended for emergency or acute care use.

Regain acts as a data processor for partner laboratories.

Processing is limited to report explanation, lifestyle execution, and patient-requested actions.