A four-tier quality system behind every product on the platform. Continuous verification, independent finished-product testing, and clinical behavior data. Every SKU must clear this baseline, and keep clearing it. Third-party cGMP certification verified for every brand and contract manufacturer (CDMO), with ongoing documentation review. Products stored in NSF cGMP-certified, FDA-registered facilities.
Fullscript-funded independent finished-product testing. ~100 SKUs per quarter, selected by our clinical team. Brands have no influence. Products must demonstrate ≥95% of label claims for potency and meet Fullscript's purity thresholds to receive a badge, valid for one year. Failures trigger root cause investigation, quarantine, and catalog removal until independently retested.
Prioritized by formulation risk, adulteration history, and intelligence from industry and academic sources on emerging concerns.
≥95% of label claims required. Confirmed by independent third-party lab.
Samples pulled from Fullscript distribution centers. Brands cannot nominate or submit their own.
Heavy metals, microbial, and novel contaminants. Fullscript holds brands to stricter microbial thresholds than industry standards.