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braun_ricks

Braun Ricks

@braun_ricks

FDA Registration Consultant, US Agent, FSVP, FDA Listing, Compliance Specialist

Vereinigte Staaten
Englisch, Französisch, Deutsch, Spanisch, Italienisch
Einige Informationen werden in englischer Sprache angezeigt.
Über mich
I help food, dietary supplement, cosmetic, and medical device companies achieve FDA compliance and enter the U.S. market confidently. With regulatory affairs expertise and hands-on experience in FDA registration, FDA listing, US Agent services, FSVP compliance, food facility registration, label review, import compliance, and regulatory documentation, I help businesses avoid costly delays, rejected filings, and compliance risks. Fast, accurate, and reliable FDA consulting tailored to your business needs.... Mehr lesen

Kompetenzen

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braun_ricks
Braun Ricks
offline • 
Durchschnittliche Antwortzeit: 254 Stunden

Meine Dienstleistungen

Technische Texte
I will prepare fda filing, fda registration, US agent and fda compliance
Ab50 $ / ProjektWeitere Details
Text & Übersetzung
I will handle fda registration, US agent, food cosmetic compliance, and label review
Ab25 $ / ProjektWeitere Details

Arbeitserfahrung

Fiverr

FDA Regulatory Compliance Consultant

Fiverr • Freiberufler

May 2022 - Present • 4 yrs 2 mos

• Assisted food, dietary supplement, cosmetic, and medical device companies with FDA registration and compliance requirements • Conducted FDA label reviews, regulatory assessments, and compliance audits • Supported clients with FDA listings, US Agent services, FSVP compliance, and import readiness • Helped businesses achieve successful market entry while reducing compliance risks and regulatory delays • Maintained a high success rate for first-time FDA registration and compliance submissions

Pfizer

Regulatory Affairs Associate

Pfizer

May 2021 - Jun 2022 • 1 yr 1 mo

• Supported regulatory submission preparation and documentation for pharmaceutical products • Assisted with FDA compliance tracking, regulatory reporting, and audit readiness activities • Collaborated with cross-functional teams to ensure compliance with applicable FDA regulations • Prepared regulatory documentation and supported product lifecycle compliance activities • Contributed to quality assurance and regulatory affairs processes supporting successful product approvals