HIPAA-Compliant Infrastructure
AWS-hosted, BAA-ready architecture with encryption at rest and in transit, audit logging, and access controls reviewed against HIPAA Security Rule controls.
8-Week MVP Launch
From idea to a production-ready, investor-grade healthcare product — with HIPAA compliance built in from day one, not bolted on at the end. Working prototype in Week 1, AI features integrated PHI-safe, and a 4-week post-launch warranty.
Trusted by global innovators
Get your 8-week launch plan in 30 minutes. We map your path, define the scope, and show you exactly what 8 weeks looks like for your product.
Is this the right solution for you?
Most healthcare MVPs take 6–12 months and still arrive without HIPAA, AI guardrails, or investor-grade documentation. We compress the timeline by treating compliance, AI, and clinical workflow as first-class engineering concerns from Week 1 — not retrofit gates at launch.
If you're building with patient data, demoing to investors, recovering from a vibe-coded prototype, or have been told a real build takes 6–12 months — this engagement is designed for you.
What you walk away with
By Week 8 you have a production-ready, HIPAA-compliant healthcare MVP — infrastructure, code, documentation, and post-launch warranty all included.
What's included in every 8-week engagement
Each 8-week engagement ships with the infrastructure, documentation, and review work hospital and investor due diligence actually asks for.
AWS-hosted, BAA-ready architecture with encryption at rest and in transit, audit logging, and access controls reviewed against HIPAA Security Rule controls.
Backend, frontend, and third-party integrations delivered as clean, maintainable code — fully yours at the end of the engagement, no licensing or escrow.
PHI-safe AI capabilities integrated from Week 1 — BAA-covered inference paths, prompt-level redaction, and audit-logged AI outputs.
BAA-ready package including audit trails, compliance reports, data-flow diagrams, and security questionnaire answers your enterprise buyers will request.
Penetration testing, automated security scanning, and a manual security review aligned to enterprise procurement checklists.
Full system documentation, runbooks, and onboarding sessions so your in-house team can operate, extend, and ship without dependency on us.
Any issues that surface in the first 4 weeks after go-live are fixed at no extra cost. You launch with confidence, not holding your breath.
Weeks 2–3 are dedicated to scope refinement — unlimited change requests included before a single line of production code is written.
Why 8 weeks works
The 6–12 month timeline isn't a law of physics — it's a symptom of waterfall scope, late-stage compliance work, and unclear ownership. We've engineered around all three.
| Dimension | Traditional 6–12 month build | Agnotic 8-Week MVP Launch |
|---|---|---|
| First working product | Months 3–6 (often a beta nobody can test) | Week 1 (fully navigable prototype) |
| Scope lock | Often unclear; bleeds through the build | Locked at Week 3 with unlimited prior changes |
| HIPAA / compliance work | Often retrofitted in the final month | Built in from Week 1 architecture |
| AI features | Phase 2 — usually pushed past v1 launch | Integrated from Week 1, PHI-safe |
| Code ownership | Sometimes escrowed or vendor-licensed | Yours — no lock-in, no licensing |
| Post-launch coverage | Billable hourly from day one | 4-week warranty included |
8 weeks is enough for a focused, investor-grade MVP. Bigger scopes roll into the 12-Week Enterprise-Ready engagement or the Healthcare Startup Acceleration subscription.
Who this 8-week engagement is for
We've shipped this engagement across women's health, behavioral health, doula workforce platforms, perinatal mental health, and clinical AI products.
Need a working product to show investors and design partners — without burning runway on a 12-month build.
Have a prototype that demos well but isn't HIPAA-safe, can't pass enterprise due diligence, or won't survive real PHI.
Need consent-aware data flows, practitioner portals, and behavioural EHR integration — built from architecture first.
Need crisis pathways, 42 CFR Part 2 aware consent, and clinician collaboration baked in — not bolted on.
Doula, therapist, or clinician workforce platforms with role-based dashboards, scheduling, and credentialing.
Founders who want AI capabilities integrated from Week 1 with PHI-safe inference paths and explainability built in.
Our 8-week MVP process
You see results in Week 1 and launch in Week 8. A phased approach with explicit gates so you know exactly what you're getting at every stage.
Step 01
A fully working prototype your team, investors, and clinical advisors can navigate and test — not a static mockup. Built in one week after 1–2 requirement clarification calls. A shared, tangible foundation before a single line of production code is written.
Step 02
Scope is locked through unlimited iteration on the prototype. Every flow, edge case, and integration is tested with stakeholders. Once Week 3 closes, production scope is fixed — protecting both timeline and budget.
Step 03
Senior healthcare engineers build the production stack on BAA-ready AWS infrastructure. Backend, frontend, integrations, AI features, and compliance scaffolding all ship in parallel. Weekly demos keep you in the loop.
Step 04
Security review, penetration testing, compliance documentation package, team training, and production deployment. You go live with full code ownership and a 4-week warranty.
After 8 weeks
The engagement doesn't stop at launch. The first 4 weeks are covered under full warranty. After that, you choose what happens next.
Any issues that arise in the first 4 weeks after go-live are fixed at no extra cost. You launch with confidence, not holding your breath.
Roll into our monthly AI + human subscription. Submit any task — features, fixes, AI work, compliance — and we deliver in 24–48 hours. Pause or cancel anytime.
When enterprise buyers ask for SOC 2, HITRUST, or FHIR integration, roll into the 12-week enterprise-readiness engagement.
What founders worry about
Challenge
What if my scope changes during development?
Agnotic approach
That's what Week 2 is for. No production code is written until scope is locked and you've tested every flow in the prototype. Change requests during Weeks 2–3 are unlimited and included — once Week 4 starts, scope is fixed to protect both sides.
Challenge
What if 8 weeks isn't enough for everything I need?
Agnotic approach
We scope to a focused, launch-ready MVP — not the full vision. Anything outside the 8-week scope rolls into Healthcare Startup Acceleration or the 12-Week Enterprise-Ready engagement. You always know what's in and what's deferred.
Challenge
Do I need a technical co-founder or in-house engineers?
Agnotic approach
No. The engagement is designed to ship without an internal engineering team. Week 8 includes a full handover, documentation, and training so you can operate independently — or roll into the monthly subscription if you'd rather keep shipping with us.
Challenge
What does HIPAA compliance actually mean in practice?
Agnotic approach
BAA-ready AWS infrastructure, encryption at rest and in transit, audit logs on every PHI touch, access controls reviewed against the HIPAA Security Rule, and a documentation package your enterprise buyers can pull straight into procurement.
Standards we build against
Every Agnotic 8-week MVP is engineered for HIPAA, BAA-readiness, and audit defensibility from the first commit. We treat compliance as architecture — never as a launch-week scramble.
Protect PHI with privacy-first architecture, encrypted storage and transmission, strict access controls, and traceable audit logs.
Implement lawful consent flows, data minimization, retention controls, and secure processing for sensitive reproductive and health data.
Enable standardized health data exchange across apps, care teams, and systems through robust FHIR-ready APIs and mappings.
Support enterprise-grade interoperability with HL7-based integrations for records, events, and clinical messaging workflows.
Align security programs to healthcare-specific controls and risk management practices trusted by providers and partners.
Design with breach notification readiness, digital record safeguards, and operational controls that support regulated care programs.
Plan software quality, traceability, and documentation pathways for products that may require SaMD review and regulatory submission.
Prepare EU market-ready processes for risk classification, evidence tracking, and lifecycle governance under MDR expectations.
Apply confidentiality controls and consent-aware sharing models for behavioral and mental health related data experiences.
With a diverse technology stack, we deliver solutions using a technology-Agnostic approach to meet your unique needs.
















We don't just build products; we forge lasting partnerships. See how we've helped industry leaders transform their vision into technical reality.
"I can clearly see how Agnotic has a unique way of handling end-to-end development. They are always active on quick chat and provide support quickly."

Founder, Benchmark
"Agnotic is the best technical team we evaluated. Their engineering excellence made our work dramatically easier and allowed us to stay focused on what matters most for maternal care outcomes. They took full ownership of the technical execution, and we are always happy to continue working together."

Founder, My Lauren
"Agnotic combines deep technical expertise with strong domain knowledge. They understand the business context, anticipate challenges, and make collaboration smooth and effective."

Founder, Latimer
Tell us your idea — even if it's still rough. We'll map your path, define the scope, and show you exactly what 8 weeks looks like for your product. Fixed scope, fixed timeline, no surprise invoices.