About Vintergatan
Meet the founder
Technical leadership and engineering services for healthcare AI. From proof-of-concept to FDA-cleared production systems.
Biography
Marcus D. R. Klarqvist founded Vintergatan Ventures to provide technical leadership and engineering services to healthcare and medtech companies. Through Vintergatan, Marcus has led technical teams from proof-of-concept through production deployment and regulatory submission. The firm's portfolio spans diverse medical AI applications. Each project delivers complete technical implementations: web applications, mobile applications and interfaces, cloud infrastructure, and embedded firmware, with comprehensive documentation for IEC 62304 and ISO 13485 compliance. These systems have achieved FDA clearance, CE marking, and UKCA approval.
Marcus holds a PhD from the University of Cambridge. Prior to founding Vintergatan, he was a founding member of the Machine Learning for Health (ML4H) program at the Broad Institute of MIT and Harvard, where he developed AI systems for clinical applications. His work has processed datasets including 100M+ clinical notes and 10M+ ECGs, resulting in 20+ peer-reviewed publications in journals including Nature Medicine and Nature Genetics. His deep expertise in both AI/ML and healthcare regulatory requirements enables him to deliver systems that are not only technically advanced but also compliant and market-ready.
Key Achievements
Deep expertise across the stack
Everything needed to go from idea to production
The boutique advantage
Direct access to experts
Work directly with our founders and senior team. No junior associates, no account managers. Just deep expertise when you need it.
Flexible engagement
From 2-week sprints to multi-year partnerships. We adapt to your needs, not the other way around.
Battle-tested playbooks
We've been through the FDA approval process. We know every pitfall, every shortcut, and exactly how to get your AI to market.
Ready to ship production AI?
Let's discuss how our expertise can accelerate your path to FDA approval
