Bring medical devices into clinical workflows faster with full-stack IoMT software. We develop patient apps, HIPAA-compliant cloud platforms, EHR integrations, and clinical analytics that help you launch with the compliance evidence regulators expect.
Build around your devices, care pathways, and regulatory requirements, not a one-size-fits-all medtech template.
Build the device layer for reliability, security, and long-term use in clinical settings.
Create RPM tools that support real clinical workflows and help care teams act faster.
Build cloud platforms that handle regulated data securely from pilot through scale.
Improve adoption with IoMT app development workstreams led by healthcare-experienced product designers.
Turn IoMT data into insights clinicians can use with confidence.
Protect patient data and stay ready for audits from the start.
Relevant builds device integration, real-time location systems (RTLS), smart-bed and infusion-pump telemetry, and centralized device management. Our IoMT solutions help hospital IT teams unify thousands of connected devices on a single, secure, EHR-integrated platform.
Relevant builds remote patient monitoring software for chronic-care providers, post-acute programs, and digital-first clinics. Our RPM platforms cover patient apps, clinician dashboards, alerting, and CMS-billable workflows for hypertension, diabetes, CHF, COPD, and post-surgical recovery.
Relevant works with medical device manufacturers developing the next generation of connected products, including wearables, implantables, smart inhalers, CGMs, and infusion devices. Our teams add the IoMT software expertise needed to accelerate delivery and support in-house engineering capacity.
Relevant builds IoMT software for decentralized clinical trials — eCOA, ePRO, sensor data capture, and integration with EDC and CTMS systems. Our IoMT integration services help sponsors and CROs reduce site burden and improve data quality.
Relevant builds telehealth and virtual-care platforms with integrated IoMT — video consultations, asynchronous messaging, and continuous device data flowing into the clinician’s view. Our IoMT platform development brings vitals, adherence, and outcomes into the same screen clinicians already use.
We bring more than 12 years of software delivery experience, having completed 246 projects for 200+ clients. Our teams have built everything from early IoMT MVPs to large-scale hospital platforms.
Our teams cover the full stack, from firmware and BLE connectivity to FHIR-based cloud platforms and clinical analytics. Engineers, cloud architects, and compliance specialists work together from day one.
We design IoMT software with compliance in mind from the start. Our work aligns with HIPAA, HITRUST, FDA, MDR, GDPR, and ISO 27001 requirements.
Our senior EU-based teams work across US and UK business hours, communicate clearly, and integrate smoothly with in-house teams. You get strong technical execution with the flexibility of a nearshore model.
We work in 2-week sprints with clear priorities, transparent backlogs, and regular checkpoints. This gives you room to adjust the scope as needs change without losing control of the budget or timelines.
The team that starts your project stays with it through delivery, rollout, and ongoing support. That continuity reduces ramp-up time and helps preserve product knowledge throughout the lifecycle.
The process starts with your devices, care pathway, users, and regulatory goals. These inputs are translated into clear requirements, success metrics, and a practical product plan.
A full IoMT architecture is mapped across devices, gateways, cloud infrastructure, apps, and integrations, with risk analysis, cybersecurity planning, and the regulatory path built into the approach.
HIPAA and ISO controls are built in early, alongside SBOMs, audit logging, and documentation that support delivery from day one.
The first production-ready release is developed for a controlled pilot, with clinical feedback used to shape the next stage of the product.
Expansion follows across sites, devices, and care pathways, supported by full integration into clinical systems and validated operational readiness.
After launch, the focus shifts to securing, improving, and extending the platform as product and regulatory needs evolve.
Connected medical device software must comply with FDA, MDR, IEC 62304, ISO 13485, and ISO 14971. Anything that touches protected health information must also comply with HIPAA. That affects how you design the architecture, run the software lifecycle, write documentation, handle cybersecurity, and address post-market obligations.
Both options are possible, and many engagements combine elements of each.
For an existing device, the work usually starts with a technical and regulatory audit covering firmware, the communication stack, cybersecurity posture, and gaps against current FDA premarket cybersecurity guidance. Based on that review, missing pieces can be added without redesigning the hardware, whether that means a modern cloud platform, patient and clinician apps, EHR integration, or AI/ML capabilities.
For a new device, support can extend across the full software lifecycle. In many cases, building on an existing device is faster and more cost-effective, but only when the current foundation meets today’s cybersecurity expectations. The right path is defined during discovery, before the project scope is finalized.
Most IoMT engagements begin with a 2 to 3-week discovery phase. This stage defines the product requirements, maps the architecture across devices, cloud, apps, and integrations, and sets a realistic MVP scope and delivery roadmap. It also clarifies intended use, product classification, applicable standards, and the cybersecurity and compliance requirements that will shape delivery.
Once that foundation is in place, the next step is usually an MVP build focused on a defined scope. Deliverables typically include a working product, architecture documentation, and a QA-tested codebase ready for deployment. After launch, support can continue through ongoing engineering work, product improvements, and post-market
A focused IoMT MVP with a single device, one care pathway, and a controlled pilot typically takes 4 to 6 months. A broader platform with multiple devices, FDA submissions, EHR integration, and clinical analytics usually takes 12 to 24 months.
Delivery runs in two-week sprints, with regulatory and clinical milestones built into the plan. That keeps progress aligned with the evidence needed at each stage.
Send us a brief about your product and goals. We will schedule a 30-minute discovery call within one business day and follow up with a fixed-fee proposal.
For more than a decade, Relevant has delivered custom healthcare software for leading organizations. Here are two examples.
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