Turn Software Chaos into Regulatory Confidence
As a CTO or team manager in MedTech, you’re juggling innovation, timelines, and compliance—all while leading a team that’s building something transformative.
But here’s the reality: even the most talented development teams can struggle when faced with the complexity of medical device regulations. Backlogs grow messy. Sprints lose focus. Documentation falls behind. And suddenly, your roadmap is at risk—not because of the tech, but because of the process.
That’s where we come in.
We specialize in bringing structure, clarity, and compliance to MedTech software teams. Our consultancy embeds directly into your workflow to:
•	Lead and align your development teams with regulatory expectations
•	Plan and manage releases that support both product goals and submission timelines
•	Administer and clean up your backlog, ensuring traceability and prioritization
•	Create focused, compliance-aware sprints that drive real progress
•	Build and maintain your Software as a Medical Device (SaMD) documentation, ready for FDA, MDR, or other regulatory bodies
We don’t just advise—we execute. We become your operational partner, helping your team daily with templates, documentation content, daily scrum, planning. 

Contact Promedee – your partner in ensuring seamless development and regulatory compliance for software as a medical device. Sleep soundly knowing your project is in expert hands: +46766363600

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