Beryl is a medical device regulatory expert specializing in regulatory strategy from premarket development to commercialization. Prior to joining Medcura, Beryl was a consultant at NAMSA and lead medical device Global Regulatory Affairs Solutions at Syneos Health where she developed clients’ regulatory strategies, lead interactions with regulatory agencies and health authorities, developed clinical trial applications, and authored final regulatory submissions.

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Beryl has worked in a broad spectrum of medical device therapeutic areas, including cardiovascular, dental, dermal, ENT, gastroenterology, general and plastic surgery, hematology and pathology, neurology, OB/gyn, ophthalmic, orthopedics, radiology, respiratory, and urology. Beryl earned her regulatory affairs certification (RAC-US) from the Regulatory Affairs Professionals Society; M.S. degree in Regulatory Affairs and Services and graduate certificate in International Regulatory Affairs from St. Cloud State University (St. Cloud, MN) ; and B.A. in Professional Communications from Metropolitan State University. (St. Paul, MN).

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