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ROBERT ERMA
@roberterma734
FDA Regulatory Consultant, 510k, Device Listing, NDC And OTC Compliance
Verenigd Koninkrijk
Duits, Engels, Frans, Spaans
Over mij
Regulatory Compliance Specialist with expertise in FDA 510(k) submissions, medical device registration, NDC drug listing, OTC compliance, FDA cosmetic registration, and EU regulatory documentation. I support medical device manufacturers, pharmaceutical companies, cosmetic brands, and startups with accurate regulatory documentation and compliance processes. Dedicated to delivering reliable, detail-oriented solutions that help businesses meet regulatory requirements efficiently and confidently.
Skills
ROBERT ERMA
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Gemiddelde reactietijd: 1 uur
Bekijk mijn diensten
Regelgeving voor medische hulpmiddelen
I will handle fda 510k submission device listing ndc and otc compliance
Certificering van productveiligheid en kwaliteit
I will handle fda mocra cosmetic facility registration and product listing
