cGP Compliance
21 CFR Part 111 demands rigorous documentation. Identity testing and master batch records must be audit-ready across thousands of SKUs.
Scale your portfolio without scaling compliance risk. We automate the technical verification of formulas, label claims, and cGMP documentation.
Managing growth in the supplement industry requires eliminating manual data entry and fragmented quality checks.
21 CFR Part 111 demands rigorous documentation. Identity testing and master batch records must be audit-ready across thousands of SKUs.
Structure/function claims require precise scientific support. AI accelerates the mapping of claims to clinical data with full traceability.
Scaling from 10 to 500 SKUs strains manual supplier management. AI automates the continuous verification of ingredient specs.
AI engines specialized for high-SKU portfolios and complex component verification.
Query your entire formula library and clinical evidence database. Get instant, sourced answers for claim substantiation and cGMP inquiries.
Learn moreProcess COAs and ingredient specs at scale. Automatically verify raw materials against master formula requirements before they hit the line.
Learn moreEnsure end-to-end traceability from raw material ingestion to final product labeling. Audit-ready reports generated in seconds, not weeks.
Learn moreBuilt and proven in the Food & Beverage industry—one of the most heavily regulated sectors on earth. We bring that same operational rigor and data integrity to Dietary Supplement manufacturing.
Schedule a personalized demonstration of how our AI solutions can optimize your workflows.