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Medical Device Regulatory Affairs Specialist FDA CE MHRA and ISO Compliance
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Medical Device Regulatory Affairs Specialist
Fiverr • Autônomo
Sep 2025 - Present • 10 mos
I provide regulatory consulting services for medical device manufacturers, importers, and distributors. My expertise includes FDA Establishment Registration and Device Listing, MHRA Registration, CE compliance documentation, UKCA requirements, ISO 13485 guidance, Declaration of Conformity preparation, and regulatory documentation. I help clients meet compliance requirements, avoid regulatory delays, and prepare products for market entry.