Liza Hantske

Principal Technical Advisor @TÜV SÜD

Carlsbad, CA, US
MOBILE NUMBERS
+19•••••••78

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WORK HISTORY

May 2024 — Present

Principal Technical Advisor @TÜV SÜD

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I provide specialized training and instruction to medical device companies, focusing on regulatory standards essential for product development and compliance. My expertise encompasses risk management, biocompatibility, quality systems, and clinical studies, guiding teams through the intricacies of each aspect. I also cover software development, design verification and validation, and audits, ensuring that every component meets the rigorous demands of the industry.I support companies in mastering the regulatory landscape, particularly for EU commerce, by delivering in-depth knowledge on medical electrical equipment and electromagnetic compatibility. By addressing these areas, I help organizations navigate complex regulations, enhance product safety, and maintain high-quality standards. My work emphasizes practical, actionable insights that drive efficiency and ensure compliance, enabling businesses to excel in a competitive market.

EDUCATION

N/A

UC San Diego

Bachelors of Science

N/A

University of Phoenix

Masters

ABOUT LIZA HANTSKE

Quality and regulatory executive specializing in regulatory strategy, quality systems…

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