Healthcare product ideas turned into production-grade MVPs in 8 to 12 weeks. Real users, real data, and a compliance posture in place from day one, on production code you won't throw away later.
Triage, intake, scheduling, or care-team consoles. Built around the one workflow that proves the model, not the kitchen sink.
First mobile or web releases for symptom tracking, telehealth, adherence, or chronic-condition support. Live in TestFlight or production, not in a Figma.
Earliest releases of SaMD candidates, device companions, or platforms heading for MDR or FDA scope. Compliance lifecycle scaffolded from day one so later certification isn't a rewrite.
First-site rollouts for clinic networks and digital health programs, with instrumentation in place to learn what to harden next.
One week. The hypothesis written down, the one workflow worth proving, the metrics that count as proof, and what is explicitly out of scope. Compliance posture set before any code.
Architecture and surface design optimized for speed without painting the next 18 months into a corner. Auth, data model, integration boundaries decided once.
Two-week sprints. Working software from sprint one, real users in pilot by week 8 to 12. CI/CD, code review, demoable progress every two weeks.
Honest read on the evidence. Double down, pivot, or stop. We support all three. The MVP is built so any of those decisions can be acted on without throwing away the codebase.
Two-week sprints, demoable software every sprint, written status notes. You own the backlog and the direction. Compliance scoping happens up front so it never blocks a release. Typical first engagements run six to twelve weeks; longer relationships continue as iteration cycles. No retainers, no team-of-one risk.
Because the first version of a healthcare product is almost never the version that scales. An MVP gets real users and real clinical data in front of the hypothesis fast enough to learn from. The discipline is in deciding what to leave out, and then building what's left properly.
Working auth, data persistence, observability, CI/CD, and a real compliance posture. No mock backends or demo-only flows, and nothing that would have to be undone before launch. Smaller scope, same engineering bar as everything else we ship.
The MVP can absolutely be HIPAA and GDPR compliant. We scope the data classification, residency, and consent flow in week one and architect accordingly. MDR or FDA pathways are longer; the MVP gets the lifecycle scaffolding in place (design history, risk file, traceability) so a later certification effort builds on it instead of starting from scratch.
First demoable build in two weeks. Pilot-ready release in 8 to 12 weeks for most scopes. Anything tighter than that, we'll tell you honestly whether it's possible and what it would cost in trade-offs.
Three paths. We keep going as your engineering partner and harden into a v1. You take it in-house with 4 to 6 weeks of pair-programming handover. Or you stop, with a clean codebase and clear documentation of what you learned. No retainers, no lock-in.
You do. Source, accounts, signing keys, and dashboards are yours from day one. We work in your repositories or hand over ours at the end. Your choice.
We'll start with a free MVP scoping conversation. Written plan, no commitment.