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beatrice_desm

beatrice

@beatrice_desm

an FDA compliance expert

Großbritannien
Englisch, Spanisch, Französisch, Deutsch
Einige Informationen werden in englischer Sprache angezeigt.
Über mich
I’m Beatrice, an FDA compliance expert specializing in FDA registration support, import permit guidance, and FDA label review for food, drug, and cosmetic products in the USA. I help businesses navigate FDA requirements through professional compliance support, documentation review, product labeling guidance, and regulatory assistance. Why choose me? I provide accurate research, attention to detail, clear communication, and personalized solutions to support your product compliance journey. Need help with FDA requirements? Send me a message today and let’s discuss your project and get started!... Mehr lesen

Kompetenzen

b
beatrice_desm
beatrice
offline • 
Durchschnittliche Antwortzeit: 4 Stunden

Meine Dienstleistungen

Gewerbeanmeldung
I will do fda registration import permit for food, drug cosmetics in USA, fda label
Produktberatung
I will handle fda 510k submission, device listing, ndc, fda registration and compliance

Portfolio

Arbeitserfahrung

Freelancer.com

FDA Drug & Cosmetic Regulatory Compliance Consultant

Freelancer.com • Freiberufler

Apr 2024 - Present • 2 yrs 6 mos

I support businesses preparing pharmaceutical and cosmetic products for the U.S. market by organizing regulatory information, reviewing documentation, and identifying applicable FDA compliance requirements. For drug products, my work includes organizing establishment registration information, drug listing data, labeler information, NDC-related documentation, product information, and labeling materials. I help clients identify missing information and prepare organized documentation for applicable regulatory processes. For cosmetic products, I assist with reviewing facility and product information, applicable MoCRA registration and listing considerations, ingredient information, labeling elements, warnings, business information, and product claims. I also conduct structured document reviews, create regulatory checklists, identify inconsistencies, and provide practical recommendations for improving compliance readiness. My work is focused on documentation quality, regulatory organization, and helping clients understand the requirements relevant to their products. I maintain a detail-oriented approach when handling regulatory information and communicate findings clearly so clients can make informed decisions about their U.S. market-entry preparation.