Software peoplewith a pharmaQA background.

Bon.do ApS is a Danish software company in Svendborg, founded in 2020 (CVR 43473425). We design and build apps, SaaS platforms, backends and connected devices, mainly for medtech, life science and healthcare companies, with quality assurance experience from the pharmaceutical industry in the same team.

Bon.do ApS is based at Rantzausmindevej 228, 5700 Svendborg, Denmark, on Funen. We work with clients across Denmark and the EU, in person or online.

Bon.do was founded by Kirsten Bondo Vraa (CEO) and Morten Bondo Vraa (CTO). Kirsten has more than ten years of experience in pharmaceutical quality assurance, including Ascendis Pharma and Sygehusapotek Fyn. Morten has more than 22 years of experience building software, from .NET and Flutter to cloud architecture and IoT. You talk directly to the people who write the code, with no account manager in between.

Yes. We build software for medtech and life science products where documentation, testing and traceability are part of the work from the first sprint: requirements trace to risks and tests, and validation records are written for your quality system. For Wear & Care we delivered a medical IoT product from design to finished backend and frontend, with MDR and GDPR requirements built in.

No. Bon.do is not ISO 13485 certified. We work inside our clients' ISO 13485 quality systems, and the regulatory responsibility stays with the client as manufacturer. Our CEO has more than ten years of pharmaceutical quality assurance experience, so we write requirements, test evidence and documentation in the form your QA expects.

Yes. We plan and document the software lifecycle to IEC 62304 and work with MDR, IVDR, GxP and GDPR requirements. We use public guidance from the Danish Medicines Agency and the EMA as input when we plan validation. Your regulatory status, such as a CE mark, stays with you as the manufacturer.

Medtech and life science companies, clinics, SaaS companies and industrial firms that need software built with the same discipline. Clients and references include Orifarm, Wear & Care, Hillerød Akupunktur, SecureFirst, Privaci, Anderup Ntech, Eimskip and MindPlus.

Every project starts with a free assessment and a written estimate, so you know the price before you commit. A focused MVP typically costs DKK 30,000–150,000 and takes 2–4 months; complex enterprise platforms start from DKK 250,000. Ad hoc senior development is DKK 800 per hour, and a dedicated team starts at DKK 400 per hour with a minimum of three months.

With a free, no-obligation project assessment that typically takes 1–2 weeks. You get a scope and requirements workshop, a project roadmap, an architecture and risk overview, and a written price estimate. If the project is not a fit, you can take the material to another team.

Yes. You do. All code, data and IP are yours from day one, built on open, well-documented tools, so you are never locked in to us. The code lives in your repository and the cloud accounts are in your name.

In the cloud region you choose, and for health data that is usually an EU region, because it keeps the compliance work simpler. We work with Azure, AWS, Google Cloud and Kubernetes. GDPR does not require EU hosting, but transfers outside the EU and EEA must meet the rules in Chapter V of the GDPR.

Yes. We work in Danish and English: meetings and documentation in either language, for clients in Denmark and across the EU.