Dr. Máire E. Ní Beilliú has held the position of Vice President, Regulatory and Quality since 2014. She leads Tricol’s Regulatory and Quality functions and is responsible for directing and overseeing the company’s global regulatory strategies. She joined the company in 2007 and prior to her current appointment Máire was Director of Operations, Research and Development at Tricol’s European division, HemCon Medical Technologies, Europe Ltd. Máire has extensive international regulatory affairs expertise overseeing numerous device registrations in the United States, Europe, and Asia / Pacific. She also has a strong R&D background with a number of scientific publications. She holds a PhD and BSc in Biochemistry from University College Dublin, Ireland.
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