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ROBERT ERMA
@roberterma734
FDA Regulatory Consultant, 510k, Device Listing, NDC And OTC Compliance
United Kingdom
German, English, French, Spanish
About me
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.
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ROBERT ERMA
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Medical Device Regulatory
I will handle fda 510k submission device listing ndc and otc compliance
Product Safety & Quality Certification
I will handle fda mocra cosmetic facility registration and product listing
