The reality on the ground
What teams in this space tell us
Conflicting ingredient frameworks
NDIs in the US, novel foods in the EU, natural health products in Canada, each market has its own positive lists, prohibited substances, and submission paths.
Health claim substantiation
EFSA Article 13/14 claims, FDA structure-function disclaimers, and TGA permitted indications all demand specific evidence formats and language.
Label complexity
Supplement Facts, NRVs, allergen statements, warnings, and quantitative ingredient declarations differ by region and need to stay aligned with the formula.
How Certo helps
Capabilities purpose-built for supplements
Formulas
Ingredient and dose validation
Check actives, excipients, and total daily doses against EFSA tolerable upper levels, FDA NDI status, and Health Canada NHPID monographs.
Claims
Permitted claim mapping
Match product claims against EFSA Register, FDA structure-function rules, and TGA permitted indications, flagging language that exceeds what the evidence supports.
Labels
Label artwork checks
Compare on-pack copy and panels against formula records, regulatory layouts, and warning requirements per market.
Documents
Dossier and notification prep
Assemble novel food applications, NDI notifications, and product license submissions from your existing supplier and stability data.
AI compliance for dietary supplement, nutraceutical, and functional food brands.
See how Certo runs compliance for teams in your space. A live demo tailored to your products takes under 30 minutes.