Entrust Your Software with Confidence
Senior expertise covering strategy, engineering, compliance, and hands-on implementation.
Services
Full ownership of your medtech software product. I take responsibility for engineering, maintenance, compliance, documentation, and day-to-day operations, ensuring the system remains stable, auditable, and aligned with standards such as ISO 13485 and ISO 27001. Designed for companies that need continuity and reliability without building a full internal team.
I support digital health teams in meeting the strict technical standards required for DiGA approval. With experience navigating TR 03161 and the full application process, I contribute directly in your codebase to implement compliant solutions or guide your technical team on how to get there.
Senior-level guidance for teams building or operating regulated software. I support decision-making across architecture, compliance strategy, quality systems, and product direction, helping you navigate standards like ISO 13485, ISO 27001, and BSI TR-03161 with practical, implementation-focused advice.
Additional engineering capacity for your software projects. I contribute directly where needed, and can extend delivery through a trusted network of experienced engineers when appropriate. All work is aligned with compliance requirements and integrated into your existing product and processes.
About
I’m a CTO and full stack software engineer with experience in medtech, working on CE-marked patient-facing applications in ISO 13485, ISO 27001, and BSI TR-03161-certified environments, with special expertise in the German DiGA (Digital Health Application) system.
Max Körlinge
Have Questions? Let's Talk
Send a quick note and I’ll get back within one business day.
You can also send an email to max@maxk.se, or contact me on LinkedIn