Experience and Expertise
MaryLou Stroumbos is executive vice president of regulatory affairs at Sirtex. She is responsible for driving the strategic direction of our global quality and regulatory affairs programs and enabling commercialization of innovative medical devices.
As a licensed attorney and regulatory affairs professional, MaryLou has supported strategic business operations and regulatory planning within the medical device industry for nearly 20 years. Before joining Sirtex in 2018, MaryLou served as director of regulatory affairs at Mitralign, Inc., where she was responsible for obtaining regulatory approvals for a novel class III cardiovascular implant device. Prior to that role she spent nine years at NxStage Medical, Inc. working in positions of increasing responsibility within the regulatory department, eventually becoming director of regulatory affairs.
MaryLou received a J.D. from Suffolk University Law School, an MBA from Rivier University, and a bachelor’s degree in business administration from the University of Massachusetts at Lowell. She also completed the Regulatory Affairs Professional Society Executive Development Program at Northwestern University's Kellogg School of Management.
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