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dave_lilly

Smith D

@dave_lilly

FDA and Compliance Expert

United Kingdom
English, Spanish, French
About me
Glad you're here!! I help U.S. and non-U.S. residents, manufacturers, importers, Amazon sellers, and brands achieve U.S. regulatory compliance. My expertise includes FDA Registration, FSVP, US Agent services, 510(k) submissions, label review, CPSIA, CPSC, and product safety compliance. I provide reliable guidance to help businesses enter the U.S. market, reduce compliance risks, and meet regulatory requirements with confidence. Looking forward to working with you soon.... Read more

Skills

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dave_lilly
Smith D
Offline • 

See my services

FDA & Food Safety Clearance
I will review your product for cpsc, cpsia, fda and safety compliance for us imports
General Legal Advice
I will do fda expert regulatory compliance legal consulting for your approval

Work experience

Self_Employed

Self Employed

Freelance • 8 yrs

FDA Regulatory Affairs and Compliance Specialist

Sep 2022 - Present3 yrs 10 mos

Provided FDA regulatory and compliance consulting services for clients in the food, pharmaceutical, and medical device industries. Specialized in ensuring compliance with FDA regulations including 21 CFR guidelines, GMP (Good Manufacturing Practices), and product safety standards. Assisted businesses with regulatory documentation, compliance strategy, quality assurance processes, and preparation for FDA audits and submissions. Supported companies in meeting U.S. regulatory requirements and improving product approval readiness.

FDA Regulatory and Compliance Consultant

May 2022 - Present4 yrs 2 mos

Provided regulatory consulting services focused on FDA compliance, quality assurance, and documentation support for food, cosmetic, and supplement products. Assisted clients in understanding FDA requirements, preparing compliance documentation, reviewing labeling for regulatory accuracy, and ensuring products meet U.S. regulatory standards. Worked closely with startups and small businesses to reduce compliance risks, improve product approval readiness, and streamline regulatory submissions.