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braun_ricks

Braun Ricks

@braun_ricks

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

United States
English, French
About me
I help food, dietary supplement, cosmetic, medical device, and international businesses navigate FDA requirements for the U.S. market. I specialize in FDA registration, U.S. Agent services, FSVP compliance, FDA label reviews, regulatory documentation, and import readiness. With regulatory affairs experience, I provide accurate, practical guidance designed to reduce compliance risks, avoid costly delays, and support successful U.S. market entry. Contact me to discuss your FDA compliance needs.... Read more

Skills

b
braun_ricks
Braun Ricks
Offline • 

See my services

Technical Writing
I will complete fda registration, US agent and fda compliance
From$50 / projectMore details
Writing & Translation
I will complete fda registration, US agent service, food and cosmetic label compliance
From$50 / projectMore details

Work experience

Fiverr

FDA Regulatory Compliance Consultant

Fiverr • Freelance

May 2022 - Present • 4 yrs 3 mos

* Support food, dietary supplement, cosmetic, medical device, and international businesses with FDA registration and regulatory compliance requirements. * Provide guidance on FDA U.S. Agent services, FSVP compliance, FDA listings, import readiness, and regulatory documentation. * Conduct FDA label reviews, regulatory assessments, and compliance checks to identify potential issues before U.S. market entry. * Help clients understand applicable FDA requirements and prepare documentation for smoother regulatory processes. * Provide practical compliance guidance designed to reduce regulatory risks, avoid preventable delays, and support successful U.S. market entry.

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. * Prepared and maintained regulatory documentation supporting product lifecycle and compliance requirements. * Collaborated with cross-functional teams to support regulatory and quality objectives. * Contributed to regulatory affairs and quality assurance activities supporting compliant product development and market approval processes.