Benjamin Kimball serves as vice president of quality and regulatory affairs for Tides, providing the company with strong expertise in multi-functional regulatory topics, quality assurance, and compliance. With more than two decades in the medical device industry — including in vitro diagnostics, bioinformatics, software/predictive algorithms, hardware, and implants — Kimball provides Tides with key insight and guidance to ensure all products meet the strictest standards for safety and quality. With strategic insights and guidance to ensure all products meet the best-in-class standards for compliance, safety, and quality.
Benjamin earned a Bachelor of Arts in microbiology and biotechnology from Notre Dame College. He went on to obtain his Juris Doctor from the Thomas Jefferson School of Law in San Diego, California.
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