GRAS in. Evidence out.
Submit your GRAS probiotic, prebiotic, or nutraceutical ingredient for real-world clinical distribution through Flore's provider network.
How the partnership works
You provide the ingredient
GRAS-status probiotic, prebiotic, or nutraceutical with stability data, CoA, and defined target indication.
We evaluate the fit
Flore reviews the ingredient against our quality gates and the indications covered by our provider network. If it fits, we proceed to partnership terms.
Clinical distribution
Your ingredient is distributed through the Flore Clinical portal to participating licensed providers. Patients are enrolled into a tracked cohort with standardized intake and longitudinal follow-up.
Outcome tracking
Longitudinal outcomes are tracked through the provider portal. Data formatted for publication, regulatory submission, or marketing claims — co-owned with the ingredient partner.
Ingredient requirements
GRAS status
Self-affirmed or FDA-notified. We do not evaluate non-GRAS ingredients or novel drug candidates.
Supply readiness
Clinical-grade packaging for the duration of the program. Stability data and certificate of analysis required.
Target indication
GI health, immune, neurological, skin, metabolic. Tell us what you're targeting and we'll assess provider-network fit.
Manufacturing standards
cGMP-compliant facility (21 CFR Part 111 for dietary supplements). Documented lot traceability.
Built for ingredient companies
Probiotic strain developers, prebiotic fiber producers, postbiotic innovators, nutraceutical formulators. If you have a GRAS ingredient and want it in front of real clinicians, this program exists for you.
Start with a conversation.
Tell us about your ingredient, your target indication, and your timeline.
Apply for Partnership →Or email support@flore.com directly