FDA Compliance for Dietary Supplements
The U.S. dietary supplement market is one of the largest in the world — but also one of the most heavily regulated. From facility registration to labeling and adverse event reporting, supplement companies must meet strict FDA requirements before products can be sold in the U.S.
At USAgentPros, we help dietary supplement brands navigate these rules and enter the U.S. market with confidence.
Key FDA Requirements for Supplements
- Facility Registration – Domestic and foreign manufacturers, packagers, and storage facilities must register with FDA.
- Label Review – Supplement Facts panels, ingredients, and claims must meet FDA rules.
- Adverse Event Reporting – Companies must track and report serious consumer complaints to FDA.
- Good Manufacturing Practices (cGMPs) – Supplement companies must follow strict production and recordkeeping standards.
- U.S. Agent Representation – Required for foreign facilities.
Our Supplement Compliance Services
- FDA facility registration and biennial renewals
- Supplement label & ingredient review
- Adverse event reporting and complaint management
- Master Manufacturing Records (MMRs) support
- U.S. Agent services for international companies
Why Supplement Companies Choose USAgentPros
Dedicated Compliance Pro – Guidance from an expert in supplements
Fast Turnarounds – Keep your launch timelines on track
100% Money-Back Guarantee – Confidence in every service
Competitive Pricing – Affordable solutions for growing brands
Bring Your Supplements to the U.S. Market
Don’t let compliance challenges slow you down. Partner with USAgentPros for simple, reliable dietary supplement FDA support.