ServiceUpdated on 24 April 2025
Regulatory project management
About
From Bench to Bedside—Expertise You Can Rely On
I bring deep, hands-on experience in guiding medical devices from concept to market. Having personally conducted and overseen all stages of preclinical testing—including in vivo studies, quality management, and regulatory submissions—I understand exactly what it takes to succeed.
As a consultant, I do this every day—supporting companies in navigating the complex path to market-ready innovation.
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- Bioeconomy
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Linda Szántó, Dr.
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