Navigate the complex world of federal and state regulations with confidence. We ensure your product is compliant from formulation to shelf.
The regulatory landscape for supplements, nutraceuticals, and food products is complex and constantly evolving. Our compliance team stays current on every requirement so you don't have to.
All manufacturing partners are fully compliant with current Good Manufacturing Practices for dietary supplements.
Every facility in our network maintains current FDA food facility registration and undergoes regular inspections.
We review product claims, marketing language, and label copy to ensure FTC compliance and avoid enforcement actions.
Supplement Facts panels, ingredient declarations, allergen statements, and required disclaimers — all properly formatted.
Many states impose additional requirements beyond federal regulations. We help you navigate the patchwork of state laws so your product can be sold nationwide.
Testing and labeling requirements for products sold in California, including heavy metals and chemical exposure warnings.
Many states require separate food facility registration and product registration. We handle the paperwork.
Several state AGs have increased enforcement on supplement claims. We ensure your marketing passes muster.
State-by-state CBD and hemp-derived ingredient compliance for products containing cannabinoids.
End-to-end regulatory support from pre-formulation to post-market surveillance.
FDA-compliant Supplement Facts and Nutrition Facts panels, ingredient lists, allergen warnings, and required disclaimers.
Identity, potency, purity, and contaminant testing through accredited laboratories. COAs for every batch.
NSF, USP, Non-GMO Project, USDA Organic, Kosher, Halal, Informed Sport, and more.
Structure/function claims, health claims, and marketing language reviewed for FTC and FDA compliance.
New Dietary Ingredient (NDI) notifications, GRAS determinations, and pre-market regulatory planning.
Amazon, TikTok Shop, Walmart Marketplace, and other platform-specific requirements handled.
Pre-audit preparation, mock FDA inspections, and corrective action plans for manufacturing partners.
Serious adverse event (SAE) reporting systems, MedWatch submissions, and post-market surveillance.
Third-party certifications build consumer trust and unlock sales channels. We guide you through the certification process and connect you with the right bodies.