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Sigrid Schoepel is an accomplished professional with extensive experience in regulatory affairs and quality management within the medical technology sector. Currently serving as the Vice President of Quality and Regulatory at EnsoData since June 2020, Sigrid maintains compliance with FDA and ISO standards while leading regulatory submissions for both new and existing products across multiple regions. Additionally, Sigrid provides regulatory consultation and technical writing services through Dirgis Professional Services. Previous roles include Director of Regulatory Affairs at HealthMyne and various managerial positions at Philips Medical Systems and ADAC Laboratories, where Sigrid oversaw technical publications for nuclear medicine and radiation therapy. Sigrid holds a Master’s in Regulatory Affairs and Services from St. Cloud State University and a Bachelor’s in English from Valparaiso University.