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Clean-label HPMC capsules for vegan-friendly brands — 8...
TingProbiotics manufactures probiotic ingredients and finished ODM/OEM products — from a 3,000+ strain library and GMP Class 10,000 cleanroom fermentation to certified capsules, powders and drops for brands in 60+ countries.
ISO 9001 · HACCP · NSF · USDA Organic — every batch traceable from strain to shelf.

Vertically integrated from strain isolation to finished packaging — measured at every step.
Four core dosage families, engineered on six automated production lines — with custom flavours, counts and branding available on every format.

Clean-label HPMC capsules for vegan-friendly brands — 8...

A 12-strain, 100 billion CFU daily capsule with DUO-CAP...

Convenient 2g stick sachets with 60 billion CFU per...

High-density lyophilised cultures from 10B to 100B CFU/g...

Pectin gummies with 5 billion CFU per serving and...

Great-tasting chewables with 20 billion CFU and prebiotic...

Oil-based drops delivering 5 billion CFU in 5 drops — the...

Thin-film strips with 2 billion CFU that dissolve on the...
Every TingProbiotics strain passes four engineering gates before it earns a production code — no shortcuts, no exceptions.
Isolation from natural sources and proprietary collections — 3,000+ strains archived, each whole-genome sequenced against safety and efficacy criteria.
Protective matrices and lyophilisation curves tuned per strain — target ≥ 90% viability retention through 24 months at 25°C.
200+ automated tanks with closed-loop pH, temperature and dissolved-oxygen control, monitored by MES with full batch genealogy.
Strain-level qPCR identity, potency, purity and stability gates — with dossiers aligned to EU, US, TGA and ASEAN registration frameworks.

Our GMP Class 10,000 plant runs six automated lines around the clock. Every fermentation vessel, filling head and packaging lane is monitored in real time — and every batch is traceable to the source strain.
A five-gate release system spans raw materials, fermentation, formulation, packaging and finished goods — with third-party verification and registration-ready dossiers for every market.
Every commercial batch is confirmed at strain level by qPCR and random WGS audit — identity is verified, never assumed.
Identity, purity, potency, moisture, safety
Real-time stability in 5 climate zones
Microbiology + heavy metals + pathogens
Across annual external certifications
A transparent six-stage collaboration — dedicated project managers, prototype samples at every milestone and complete documentation in hand before production starts.
Target market, claim strategy and volumes become a formulation brief — with strain options and regulatory mapping in 3 business days.
Strain blend, dosage form, flavour and stability design — working prototypes in your hands within 30 days.
Pilot batches validate the process at production scale while stability chambers begin 24-month shelf-life studies.
GMP production on automated lines with in-process checks at every gate — fermentation through final packaging.
COA, strain identity reports and registration dossiers ship with every order — no chasing paperwork.
Door-to-port logistics, complete export documentation and dedicated support for reorders and market expansions.
Tell us about your project — target market, dosage form and estimated volumes. Our product team replies within 24 hours with formulations, samples and a tailored proposal.
Send your target market, dosage form and annual volumes. Our team responds within 24 hours with formulation options, samples and a complete quotation.