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Claire W
@claiirewilson
United States
English, Spanish, French, Arabic
About me
I am a Regulatory Affairs & Medical Writing Consultant with 7+ years of experience preparing FDA 510(k) documentation, medical device compliance reports, and regulatory submissions. I’ve worked on Class I, II, and III devices, supporting startups and global manufacturers in getting their devices cleared for the US market.
I deliver clear, structured, and compliant reports with attention to FDA guidance, ensuring your documentation meets regulatory expectations.
Skills
Claire W
Offline •
Average response time: 10 hours
See my services
Research & Summaries
I will prepare and assist with fda 510k documentation for medical devices
Business Strategy & Innovation
I will provide fda facility registration and US fda compliance
