Sarah directs medical device and IVD consulting for NSF. She has more than 20 years of professional experience, including with quality management systems, regulatory compliance (U.S. FDA and EPA, Health Canada, EU MDR and IVDR, China NMPA), business mergers and acquisitions, continuous improvement, new product submission, product recall and remediation, people management, and process management. Both large and small international and culturally diverse companies have offered her a wide range of business experience over her career.
In addition to her work in the medical device industry, Sarah is passionate about nonprofit organizations in the St. Louis region that offer support for safe housing, health care and education. She has volunteered time with Doorways interfaith residences, Springboard to Learning and the DePaul Health Care Foundation. In addition, Sarah is proud to have been a part of the FOCUS St. Louis 2015-16 leadership class, working to better the St. Louis region through a commitment to the community.
Sarah holds a bachelor's degree in chemical engineering from the University of Missouri-Columbia.
Areas of Expertise
- Global Medical Device Regulations
- Quality Management Systems
- FDA Remediation Support – 483, Warning Letter and Consent Decree Response and Recall Support
- Mergers and Acquisitions Diligence Support
- Audits & Inspections
- Client Management