Who we are
In the vibrant realm of MedTech, where innovation is the heartbeat of progress, our SME stands as a beacon of expertise and creativity. With our profound knowledge in research and the art of new product development, we become the indispensable ally for corporate entities eager to expand their product portfolios. As architects of solutions and systems for Software as a Medical Device (SaMD), we design with precision and a visionary touch. Our commitment to excellence is further certified by our implementation of robust Quality Management System (QMS) principles, ensuring that our trusted collaborations deliver not just products, but pioneering advancements. Join us in crafting the future of medical technology, where every project is a masterpiece in the making.
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MedTech System Architecture
We engineer interoperable, secure, and scalable systems that connect devices, data, and decision-making — from concept to compliance.
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Regulatory-Ready Innovation
From ISO 13485 to IEC 62304 and ISO 27001, our workflows are built with certification in mind — enabling faster market entry with confidence.
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Project Readiness Index
We use a maturity and compliance framework to assess your MedTech product’s readiness for certification and deployment.
The Project Readiness Index reflects:
- Functional completeness
- Regulatory alignment (ISO 13485 / IEC 62304)
- UX/HFE and cybersecurity readiness
- System integration & scalability
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Sustainable Design Commitment
We embed eco-conscious choices into every design decision — from code efficiency to hardware selection.
Our Sustainable Design Score considers:
- Energy-efficient runtime performance
- Use of eco-certified components
- Modular, repairable architecture
- Low-bandwidth cloud integrations
Our Quality & Security Certifications
As part of our commitment to regulatory excellence, Moebiusol SRL maintains three internationally recognized management certifications. These ensure that our solutions meet the highest standards for quality, medical device safety, and information security.
Project Readiness Index
We use a maturity and compliance framework to assess your MedTech product’s readiness for certification and deployment.
The Project Readiness Index reflects:
- Functional completeness
- Regulatory alignment (ISO 13485 / IEC 62304)
- UX/HFE and cybersecurity readiness
- System integration & scalability
United Nations procurement
Moebiusol SRL is registered as a supplier on the United Nations Global Marketplace (UNGM), supplier number 1226866.
This registration enables Moebiusol to identify and participate in relevant procurement opportunities across the United Nations system, subject to the eligibility, qualification and contractual requirements of each issuing organization.
Our procurement-readiness framework is supported by controlled company governance, professional-conduct principles, quality and information-security management systems, supplier assurance, traceability and corrective-action processes.
Moebiusol acknowledges the UN Supplier Code of Conduct and is committed to ethical, transparent and accountable participation in international procurement.
UNGM registration does not constitute endorsement by the United Nations or guarantee eligibility or selection for an individual procurement opportunity.
Why choose us
Design with Purpose. Precision with Soul.
Great design isn’t a phase — it’s the foundation. We create MedTech solutions that are intuitive, regulation-ready, and aesthetically refined.
Our work is guided by standards like IEC 62366 and ISO 13485, but driven by empathy and user-centered design.
From early visual workflows to modular, scalable architectures, we blend creativity with constraint — turning complex compliance into elegant user experiences.
We don’t just deliver products; we co-create solutions with you, embedding strategy and innovation in every design decision.
Partner with us to shape technology that feels as natural as it is powerful.
Human-Centered by Design
Every pixel, every interaction — crafted with empathy. We apply UX principles and clinical insights to build systems that are as intuitive as they are powerful.
Standards-Aligned, Innovation-Fueled
From ISO 13485 to IEC 62304, compliance is baked into our process — not bolted on. We turn regulatory boundaries into launchpads for breakthrough ideas.
Our Solutions
Smart. Scalable. Standards-Aligned.
Cloud-native and ISO 13485-ready, our platforms deliver precision, safety, and performance for regulated digital health products. We specialize in standalone software that meets the definition of a medical device, including clinical calculators, diagnostics, and remote monitoring.
We bridge the physical and digital with real-time, edge-to-cloud data flow for biosignals, vitals, and environmental context. Our solutions integrate seamlessly into consumer or clinical-grade wearables, enabling continuous monitoring with privacy and compliance in mind.
Compliance in Code. Clarity in Data.
Designed with clinicians and patients in mind, our UIs surface real-time health insights in clear, usable formats. Whether it's a professional monitoring console or patient companion app, we prioritize trust and clarity.
Our systems come with built-in support for ISO 13485, 14971, 62304, and 27001. We deliver traceability matrices, audit logs, documentation frameworks, and architecture rationale — ready for regulators.
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Some of Our Esteemed Clients
