Sarah Moore 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, Health Canada, EU MDD(R)/IVDD(R), U.S. EPA, CHINA NMPA), business mergers and acquisitions, continuous improvement, new product submission, product recall and remediation, risk management, process management, and people management. Both large and small international and culturally diverse companies have offered her a wide range of business experience over her career. Sarah believes people are the most critical resource that drives business, and she focuses her efforts and attention on building relationships first. When strong trust is built, healthy and profitable business always follows.
In addition to her work in the medical device industry, Sarah is passionate about non-profit organisations in the St. Louis region focused on community betterment. She has volunteered time with several community organisations that bring greater access to housing, health care and education, and is always on the lookout for opportunities that contribute to improving human health, both locally and globally.
Sarah holds a Bachelor of Science in chemical engineering from the University of Missouri - Columbia.
Areas of Expertise:
- Global Medical Device Regulations
- Quality Management Systems
- U.S. FDA Remediation Support – 483, Warning Letter, and Consent Decree Response and Recall Support
- Mergers and Acquisitions Diligence Support
- Audits and Inspections
- Client Management