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Sobre mim
With expertise in UK, US, & European regulatory frameworks, I assist manufacturers, distributors, & importers in navigating complex regulatory pathways. My core competencies include UK MHRA Account Setup & Device Registration, UKCA Mark Compliance, UK Responsible Person (UKRP) Guidance, FDA Facility Registration/510(k), and EU MDR Technical File Compilation.
Do you need product classification, GMDN/NMiD mapping, or full registration submissions, I provide accurate, turn-key solutions to ensure your product remains 100% compliant.
Send me a message today for professional compliance guidance... Saiba mais