FORNUTRA operates under recognized quality and food safety systems, holding GMP, ISO 22000, and HACCP certifications plus an FDA certificate. Our manufacturing follows standards aligned with FDA and EFSA requirements, and we provide documentation to support US and European market entry. One important point: dietary supplements are regulated differently from drugs, so no supplement manufacturer i...

FORNUTRA confirms specifications, formula and ingredient documents, batch COAs, test reports, production or quality system files, commercial invoices, packing lists, origin-related documents, and label information based on the product and country of sale. US and European requirements differ, and EU member states may add notification, language, and ingredient restrictions, so a project-specific d...

FORNUTRA provides the base information needed for formulas, ingredient specifications, production, batch quality, testing, and labeling, and supports US or European document preparation on a project basis. US projects should not be described as FDA-approved; European projects require separate review of ingredients, dosage, country of sale, label language, and health claims. Final label and marke...

Multi-Country Ingredient Compliance Managing multi-country ingredient compliance starts before formulation begins. At project initiation, we ask clients to specify their target markets so we can align the formula and ingredient selection with all applicable regulatory frameworks simultaneously — rather than formulating first and checking compliance later. Our approach combines three layers: form...

Quality and Compliance Standards at FORNUTRA FORNUTRA operates under a structured quality management system built on three pillars: Good Manufacturing Practice (GMP) guidelines, HACCP-based food safety protocols, and a documented quality management system that governs every stage from raw material intake to finished product release. Our GMP framework follows international supplement manufacturin...