
Elizabeth mercy
FDA Regulatory Compliance Specialist 510k MoCRA FSVP and US Agent Services
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FDA Regulatory Affairs Specialist
Business • Freelance
Mar 2026 - Present • 2 mos
As an FDA Regulatory Affairs Specialist, I manage FDA 510k submission, FDA registration, and medical device compliance for startups, manufacturers, and Amazon sellers entering the US market. I have successfully guided multiple clients through premarket submissions, ensuring accurate documentation and regulatory alignment. My responsibilities include device classification, FDA device listing, US agent coordination, and NDC registration. I work closely with clients to prepare complete, error-free submissions that reduce delays and improve approval success rates. I have helped businesses avoid costly FDA rejections, compliance penalties, and Amazon listing issues by providing clear, strategic regulatory guidance. My focus is on fast turnaround, compliance accuracy, and delivering results that support product approval and market entry.