supplements. nutraceuticals. probiotics. botanicals.
23,00023,000emergencyemergencyroomroomvisitsvisitsaayear.year.Two-thirdsTwo-thirdsofofproteinproteinpowderspowdersexceedexceedsafesafeleadleadlevels.levels.89%89%ofofperformanceperformancesupplementssupplementsmislabeled.mislabeled.TheThesupplementsupplementindustryindustryhashasaaformulationformulationsciencescienceproblem.problem.
Ceuvita brings pharmaceutical-grade formulation science to supplement, nutraceutical, probiotic, and botanical brands. Every ingredient is selected from published clinical research. Every interaction is screened. Every claim is backed by a regulatory-ready evidence dossier.
Ceuvita starts every formulation with published clinical research. Ingredient selection, dosing, and form are all chosen based on peer-reviewed evidence.
12% of supplements contain FDA-prohibited ingredients. Drug-supplement interactions send thousands to the emergency room every year. Every Ceuvita formulation includes complete interaction screening, ingredient to ingredient and ingredient to drug.
EFSA rejected roughly 80% of health claims submitted to it. Ceuvita delivers a full evidence dossier with every formulation: clinical backing for every claim, safety documentation, and regulatory alignment for your target markets.
Supplements are the fastest-growing segment of consumer health. The science behind most formulations hasn't kept pace with the marketing. And the consequences are real.
of protein powders tested exceed safe lead levels.
Consumer Reports, 2025emergency department visits per year from supplement adverse events. Only 2% are reported to the FDA.
of performance supplements carry inaccurate labels.
older adults using supplements with prescription medications are at risk of serious interactions.
in annual US supplement sales with no requirement for pre-market safety testing by the FDA.
Nutrition Business Journal, 2024The supplement industry has a formulation science problem.
Our Commitment
Ceuvita exists to make pharmaceutical-grade formulation science accessible to every brand willing to hold itself to a higher standard.
Join the waitlist for early access to Ceuvita. Pharmaceutical-grade formulation science and regulatory-ready documentation, delivered in 5 to 15 days.
