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wisdomjoshua1

Wisdom J

@wisdomjoshua1

FDA Registration and Compliance Specialist

Estados Unidos
Inglês, Alemão, Espanhol, Francês
Algumas informações são exibidas no idioma inglês.
Sobre mim
Hello, I’m Wisdom, founder of Wisdom Regulatory Services, Compliance, and Gov’t Contracts. I help startups, manufacturers, and international businesses successfully enter and operate in the U.S. market without regulatory stress. From FDA registration and product listing to SAM.gov setup, I ensure your business is fully compliant, accurate, and ready for opportunities. I focus on simplifying complex processes, preventing costly errors, and delivering fast, confidential, and reliable support so you can focus on growing your business with confidence.... Saiba mais

Habilidades

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wisdomjoshua1
Wisdom J
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Tempo médio de resposta: 2 horas

Conheça meus serviços

Upload de Produto
I will do fda registration and product listing
Autorização de segurança alimentar e da FDA
I will fda compliance, product listing and US agent service

Portfólio

Experiência profissional

Freelancer.com

Regulatory Compliance Specialist

Freelancer.com

Apr 2026 - Present1 mo

Description: Provide regulatory compliance support to startups, manufacturers, and international businesses seeking entry into the U.S. market. Specialized in FDA registration, product listing, and compliance guidance for food, cosmetics, and medical devices. Assist clients with U.S. Agent representation, documentation, and submission processes to ensure accuracy and regulatory alignment. Also support SAM.gov registration and government contract readiness. Focus on simplifying complex requirements, preventing costly errors, and delivering reliable, confidential, and timely solutions tailored to client needs.

HealthCare.gov

FDA Medical Device Listing Support for Startup Manufacturer

HealthCare.gov

Mar 2026 - Present2 mos

A medical device startup required assistance with FDA listing requirements before launching their product in the U.S. market. Their main concern was ensuring proper classification and compliance documentation to avoid regulatory delays. I provided structured guidance on FDA medical device listing requirements, helping the client organize their product classification details and prepare necessary submission data. I also supported them in understanding compliance pathways relevant to their device category. The project was successfully completed, giving the client a clear compliance roadmap and readiness for U.S. market entry.