we learn your world
Before we write a line of production code, we invest time understanding your product, your processes, and your domain. In medical laboratory work, that has literally meant going on-site to labs and watching how analysts work.
We adapt our development process to your preferences and project requirements, using methodologies such as Agile and Waterfall.
Depending on each case, project roles can be covered exclusively by the RomSoft team or in tandem with the customer team.
For application life cycle management we are mainly using Azure DevOps Server (ADOS) but we can easily adapt to other systems that our customers are comfortable using. We have solid experience using Confluence, Jira, Polarion and CodeBeamer.
we work as one team
Your tools, your rituals, your codebase conventions. We adapt to your workflow. RomSoft engineers participate in architecture decisions and planning – not just ticket resolution. The difference shows over time.
we grow with you
The engineers who built earlier versions of your product continue to evolve it. They know the decisions made two – or twenty years ago, and the reasoning behind choices that aren’t obvious from the code. The knowledge compounds. Our longest partnership has run for 25 years – because the engineers who started on the product continue to evolve it, carrying context that doesn’t reset.
science & tech,
together
25 years of building software where the regulatory context was never an afterthought – available at engagement sizes that EU health-tech companies can actually reach, from an EU member state with no geopolitical risk. Your IP stays yours. Our commitment stays long.
We work at the intersection of software engineering discipline and deep domain knowledge. The projects we take on are the ones where that combination genuinely matters.
Regulated software is a different discipline. We are ISO 9001 certified, TÜV Austria. Our quality management system is independently audited. ANCS R&D certified. Microsoft Gold Partner.
We have delivered software for Class B and Class C medical devices – the higher risk classifications under IEC 62304. We can discuss what that means for your product in a first conversation.
R&D & EU-funded projects – Since 2008, we participated in 13 R&D projects over 13 years, across e-health, telemedicine, disease self-management, AI/ML, and blockchain. This is how we stay ahead in technologies that aren’t yet mainstream – and how our clients benefit from early capability depth.