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Vienna, March 2026 – Erbe Elektromedizin GmbH, a leading German medical device manufacturer, has been awarded the Microsoft Intelligent Manufacturing Award (MIMA) 2026 in the Small and Medium Enterprise (SME) category. The award recognizes the successful implementation of Flinn’s AI-powered literature evaluation solution, developed in collaboration with Erbe and deployed as part of the project EvidenceStream, to automate and transform clinical literature evaluation processes.
Selected from hundreds of applicants, Erbe and Flinn advanced to the final round of 15 companies and presented the solution during the final pitch session. The project stood out for its ability to combine regulatory rigor with cutting-edge AI to drive measurable operational impact.
Transforming Regulatory Intelligence with AI
EvidenceStream enables the automated extraction and structuring of clinical evidence from scientific literature, addressing one of the most time-intensive processes in medical device compliance.
Developed in partnership with Flinn, the platform applies intelligent screening and extraction agents to conduct systematic, comprehensive, and reproducible literature searches in full alignment with EU Medical Device Regulation (MDR) requirements. The system is currently deployed across more than 60 device groups.
The results demonstrate significant efficiency gains:
Importantly, these efficiency gains were realized without workforce reductions, allowing Erbe to reallocate resources toward higher-value scientific analysis and strategic decision-making.
A Partnership Built on Trust and Execution Speed
The collaboration between Erbe and Flinn combined deep regulatory expertise with advanced AI engineering, enabling rapid deployment from concept to production.
Prof. Dr. Markus Enderle, Chief Scientific & Medical Officer and Member of the Executive Board at Erbe Group, commented:
“Flinn understood from day one that our goal was not automation for its own sake, but building a system our experts would trust. Their combination of AI engineering and our regulatory expertise and experience made EvidenceStream possible to come to life from contract to production in eight months. That speed, paired with measurable results, is why we see this as a long-term partnership.”
Prof. Dr. Nermin Salkic, Global Medical Director at Erbe Group, added: