University-partnered R&D, on-site QC lab, and a 6-step process that ships only what we can defend
Every claim on this site is backed by a registered IP, a documented process, and a third-party lab report. Our technical team develops every formula — and we let you audit every step of how it gets to your customer.
In-house R&D, backed by university partnerships
Our in-house technical team is responsible for every formula on this site — from the bio-enzyme + probiotic deodorizing complex to the stabilized chlorine dioxide disinfectant system. We don't white-label third-party formulas and we don't pass through generic bases.
In addition to our internal team, we maintain active R&D cooperation with partner universities in formulation chemistry, microbiology, and packaging engineering. This gives us access to academic literature, validation methods, and a pipeline of graduate-level researchers for the custom formula projects that go beyond catalog.
What we measure in-house, before we ship
Our on-site lab handles routine QC. For final claim verification (kill rates, allergen removal, probiotic counts) we use independent third-party labs — reports published in full.
pH & conductivity
Every batch. Calibrated daily. Recorded in the batch ledger.
Microbial limits
Total plate count, yeast & mold, E. coli, S. aureus, P. aeruginosa — per pharmacopeia.
Active content
Chlorine dioxide concentration, enzyme activity, probiotic CFU counts.
Stability & aging
Accelerated aging at 40°C / 75% RH. Long-term shelf-life validation for new SKUs.
From incoming raw material to packed carton
Every batch is traceable end-to-end. If a claim ever needs defending, we can produce the full documentation chain in under an hour.
IQC · Incoming Quality Control
Every raw material lot is sampled on arrival. COA from supplier is verified against in-house re-test for identity, purity, and microbial load. Non-conforming lots are rejected and isolated.
REJECT-RATE TRACKEDFormula batching
Mixing & blending under validated process parameters: temperature, RPM, vacuum, hold time. Batch records captured digitally and counter-signed by the line supervisor.
DIGITAL BATCH RECORDIPQC · In-Process Quality Control
pH, viscosity, active content, and visual checks at pre-defined checkpoints. Out-of-spec batches are quarantined before filling — not after.
CHECKPOINT-LEVELFilling & packaging
Class-D cleanroom filling with online particle counting. Fill-weight verification, torque testing on caps, leak detection, and visual inspection on every unit.
UNIT-LEVEL TRACEOQC · Outgoing Quality Control
Final sampling per AQL. Microbial limits, active content, appearance, pH, and packaging integrity. Only lots that pass every OQC check are released to the warehouse.
AQL SAMPLING3rd-party claim verification
For every claim published on this site (94.2% ammonia removal, 99.999% kill rate, etc.) we commission an independent lab. Reports are public and PDF-downloadable.
INDEPENDENT LABEvery claim has a paper trail. Every paper trail is downloadable.
Regulatory, import, and retail compliance all depend on consistent documentation. We provide the full set with every shipment and on-demand for prospect clients.
MSDS
Material Safety Data Sheet for every SKU. Bilingual EN/中文 where required.
COA
Certificate of Analysis for every production batch, with lot number and test results.
Third-party lab report
SGS / equivalent independent lab verification of every claim on the product page.
FDA registration
Facility registration confirmation and product listing details for the US market.
ISO 22716 GMP certificate
Cosmetic GMP scope certificate from our certification body. Audit report available under NDA.
Customs & export documents
Commercial invoice, packing list, certificate of origin, and HS codes prepared for every shipment.
For the full document set under NDA, contact your account manager →
Your formula, our lab — under NDA, on a documented timeline
For OEM projects, our R&D team starts from your spec — target performance, ingredient preferences, regulatory targets, and target cost. We sign a mutual NDA before any formula or spec exchange.
Typical OEM project: 30–45 days from spec acceptance to lab sample, then another 15–25 days for pilot batch and stability. Your formula, your IP — we sign an IP assignment at project kickoff.
- ✓ NDA signed before any spec exchange
- ✓ IP assignment at project kickoff — formula belongs to you
- ✓ Stability data provided before commercial order
- ✓ Compliance hand-off for FDA, EU, and target-market filings
Custom project timeline
-
1
Spec & NDA · 2–3 days
-
2
Lab formulation · 10–15 days
-
3
Sample & approval · 5–7 days
-
4
Pilot batch & stability · 15–25 days
-
5
Commercial run · 15–45 days