Revolve Healthcare

Revolve Healthcare is a Polish software development company focused exclusively on regulated medical products. They work with medical device manufacturers, MedTech startups, pharma companies, hospitals, biotech firms, and mental health providers building software that requires FDA, MDR, or CE certification. The company holds ISO 13485 certification, meaning they operate their development process under the quality management system required for medical device software. Their client roster includes ylah, Innovation Zed, Innitius, ENPICOM, and obvioTec—all building regulated products.

The team combines software engineering with regulatory expertise. Rather than bouncing between industries, Revolve stays in healthcare, which shapes how they approach every engagement: from product design through post-market maintenance. Several team members have academic backgrounds in technical domains, allowing them to engage with complex scientific and engineering problems. One founder is named Przemek (full name not provided in source).

Services and capabilities

Revolve builds four core deliverable types: mobile apps (React Native, Swift, Kotlin), web platforms (.NET, Python, TypeScript), desktop software, and firmware or embedded systems. They also do product design starting at the early concept stage, quality assurance audits, cloud and DevOps for healthcare, regulatory consulting (MDR, MDD transition, IVDR), and cybersecurity and data privacy work.

Mobile app work includes companion apps for medical devices, patient monitoring platforms, and therapy apps. Web platforms range from standalone solutions to systems that integrate with hospital EHR and HIS systems. They use AWS, Microsoft Azure, and Google Cloud Platform. Desktop software targets medical device control, data analysis, diagnostics, and lab workflows—built with scalable architectures that support HL7 FHIR standards and MDR compliance.

Firmware and embedded work connects devices to companion apps and cloud platforms. Product design clarifies user needs, regulatory constraints, and technical feasibility early, and can include clickable prototypes for fundraising. The company supports clients through MDD-to-MDR regulatory transitions and acts as a "critical software supplier" documented in clients' regulatory submissions.

They serve six vertical markets: medical device (diagnostics, monitoring, digital therapeutics), biotech (clinical trial software, lab journals), pharma (quality control systems, pharmacy CRM), mental health (therapy platforms, cognitive optimization tools), laboratory (data collection and analysis), and veterinary.

Notable work

Clients named in the source include ylah (building a regulated medical platform, with CEO Florence von Gunten crediting Revolve for "deep understanding of medical software compliance and user experience"), Innovation Zed (CEO Dean Minnock noting the team's "dedication, precision, and shared ambition"), Innitius (building Cervisense, an OB/GYN web app for MDR and cybersecurity compliance), ENPICOM (CTO Jorrit Posthuma praising "competent and committed" developers and "excellent communication and good English"), and obvioTec (a data science firm where Revolve automated a process that reduced measurement time from a week to one day using Python).

Project examples from their site include: medical device firmware refactors, mobile and web apps for chronic kidney disease home monitoring, a centralised health information system for Iceland's Ministry of Health, a blended therapy platform for psychotherapists and patients, diagnostic medical device firmware, and a desktop app automating pharmaceutical quality control for laboratories.

How they work

Engagement begins with a free 45-minute discovery call reviewing product concept, regulatory context, and technical scope. Revolve then prepares a project proposal with scope, timeline, and delivery model. After agreement and legal setup, a dedicated team integrates into the client's workflow and development environment.

The company positions itself as a "critical software supplier" within clients' regulatory frameworks. This means Revolve documents its development process, testing, and cybersecurity practices to be included in the client's MDR or FDA submission. They handle software-level testing and safety analysis; clients retain final decision-making on product-level testing and overall regulatory coordination. Revolve provides technical documentation, ongoing maintenance, and post-market support including updates and data to support product management.

No pricing or typical project duration is disclosed in the source, though they mention delivering "the first working solution in 3-6 months" using Agile methodologies for mobile apps.

Team and credentials

One team member is named Przemek (founder, first name only in source). The source does not disclose total team size. Revolve holds ISO 13485 certification (medical device QMS). They claim familiarity with ISO 27001 (information security), IEC 62304 (medical device software lifecycle), and IEC 62366 (usability standards). Clients cite "excellent communication and good English" as a working strength. The company mentions "multiple skilled people within our team" with academic backgrounds but provides no headcount, office locations, or hiring timelines.