Probiotical S.p.A.
Italian maker of lyophilized and microencapsulated probiotic strains plus finished probiotic products.
- MOQ
- Not publicly disclosed
- LEAD TIME
- Not publicly disclosed
Overview
Probiotical is an Italian dedicated probiotic-microorganism manufacturer headquartered in Novara, Piemonte. Founded in 1985 with origins tracing to a 60-year heritage in lactic acid bacteria for the dairy industry, Probiotical operates an Italy plant designed exclusively for probiotic microorganism production for pharmaceutical and nutraceutical applications. The company's portfolio includes lyophilized and microencapsulated probiotic strains plus finished probiotic products. Probiotical is distinct from Probi AB (Swedish probiotic company already listed in Inventory Ready) — different companies, different countries, no parent overlap.
Certifications
Certification verification in progress. International supplier records require regional database lookups (EudraGMDP, Health Canada NHP, FSSC public register, JHFA directory). See our methodology.
Capabilities
- PRODUCT TYPES
- Lyophilized Probiotic Strains · Microencapsulated Probiotic Strains · Lactic Acid Bacteria Cultures · Finished Probiotic Products · Probiotic Raw Materials for Pharma + Nutraceutical Use
- CAPABILITIES
- Probiotics or postbiotics · Delivery or absorption technology · Pharmaceutical-grade production · Also makes finished supplements
Sources
What we couldn't verify
We did not visit this company on site. See the limits that apply to every listing.
- FSSC 22000 explicit status (ISO 22000 confirmed; FSSC may also be held but not surfaced)
- ISO 14001 environmental management (vendor lists; not in IR's canonical certifications.json — verify and add to taxonomy if confirmed)
- Per-strain identity-testing method documentation
- Strain-deposit registry references
- PACER + Italian court direct-litigation query
- FSSC 22000 still not claimed by the vendor as of the 2026-08-12 re-review: its own certifications page lists Ecovadis, ISO 22000:2018, ISO 9001:2015 and ISO 14001 (all Jas-Anz) and no FSSC. ISO 22000 alone satisfies the EU regulatory equivalent gate per inclusion-criteria.json
- Probiotic-strain quality-control specifics (strain-identity testing methods, stability data) not surfaced in this pass — buyers should request COA samples + strain-deposit registry references at first engagement
- EU regulatory framework differs from US 21 CFR Part 111
- AIFA (Italian medicines agency) direct-query deferred — Probiotical positioned in food/supplement scope, not pharma
Dietary supplement manufacturers must comply with 21 CFR Part 111 (cGMP). What Part 111 requires
The connection map between Probiotical S.p.A. and other vendors, capabilities, and certifications is in the manufacturer atlas.
Enforcement screening: included in Inventory Ready's most recent completed pass against FDA's published recall datasets (2026-07-09). Method and limits →
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