Will Sammons is currently the Associate Director of Global Regulatory Affairs for Software, Digital Health, and Cybersecurity at Baxter International Inc., where they oversee regulatory compliance and strategy for medical device software. With 19 years of experience in safety, regulatory, and quality engineering, they have a robust background that includes previous roles at companies such as Hillrom, Intertek Testing Services, and Circassia. Will holds a Bachelor of Science degree from North Carolina State University, enhancing their expertise in FDA regulations and international standards for medical devices. Their specialties encompass the creation and submission of FDA 510(k) applications and quality assurance across hardware and software life cycles.
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