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Dorcas J
@dorcas_jasmine
FDA Registration, Compliance, US Agent and Label Review
Nigeria
Englisch
Über mich
Hello, I’m Dorcas Jasmine, an advanced FDA registration Agency. I'm dedicated to helping businesses work out U.S. Food and Drug Administration requirements with clarity and confidence. I offer support with FDA registration, food facility registration, product labeling, and regulatory documentation, prioritizing accuracy, clear communication, and attention to detail. I believe quality service begins with honesty, reliability, and understanding your needs. Send me a message today, and let’s discuss how I can support your project with a tailored, professional approach. CHEERS TO HUGE SUCCESS.
Kompetenzen
Dorcas J
offline •
Durchschnittliche Antwortzeit: 1 Stunde
Meine Dienstleistungen
Zertifizierungen und Vorschriften
I will handle fda compliance, fda registration, US agent service, fsvp agent and label
Text & Übersetzung
I will handle fsvp, fda registration, US agent service, label review, fda compliance
Arbeitserfahrung
Position: FDA Regulatory Compliance Specialist Company: Independent Consultant / Self-Employed
Freelancer.com • Freiberufler
Feb 2021 - Present • 5 yrs 9 mos
As an FDA Regulatory Compliance Specialist, I help businesses understand US Food and Drug Administration requirements and prepare for the US market. My work covers FDA registration, FDA compliance, product listing, label review, food facility registration, US Agent requirements, import compliance, and regulatory documentation for food, dietary supplements, cosmetics, drugs, and medical devices. I support product brands, manufacturers, importers, startups, and international businesses seeking clear guidance on FDA requirements. My services include reviewing food labels, supplement labels, cosmetic labels, ingredient information, and product claims to identify potential compliance concerns. I also provide guidance on MoCRA cosmetics compliance, Foreign Supplier Verification Program (FSVP) requirements, drug establishment registration, NDC listing, medical device listing, and applicable 510(k) submission processes. Every project begins with understanding the product category, business goals, and specific regulatory needs. I help clients organize relevant information, identify documentation gaps, understand applicable requirements, and determine practical next steps. I focus on clear communication, careful document review, attention to detail, and solutions tailored to each project. My goal is to make complex FDA requirements easier to understand and help businesses approach regulatory responsibilities with greater confidence. Whether a client needs an initial compliance assessment, product label review, registration guidance, or support understanding US import requirements, I aim to provide clear information and professional assistance throughout the agreed scope of work. I understand that FDA requirements vary depending on the product, intended use, facility, and business activities. For this reason, I approach each project individually rather than relying on a one-size-fits-all solution. I prioritize accuracy, transparency, responsible guidance, and professional
