Inside the Factory Behind Your Brand
We manufacture skincare for brands in 50+ countries from this facility in Dongguan, China. GMP ISO 22716 certified. Audit-ready at all times. Every section below comes with a document you can request.
Virtual audits available within 5 business days · Physical visits welcome with advance notice
Facility Overview
Our Dongguan facility was purpose-built for cosmetic manufacturing and has been continuously upgraded since 2000. The facility operates 6 days per week with full cleanroom protocols enforced at all times. We welcome virtual and physical audits from B2B buyers at any stage of the sourcing process.
Key Specifications
GMP Cleanroom — 100,000-Level
Our primary manufacturing area operates at 100,000-level cleanroom purity — the international standard for cosmetic manufacturing compliance. Temperature and humidity are continuously monitored and logged. All production staff pass health checks and PPE compliance before entering. This is the standard that EU, US, and Middle East regulators expect when they audit a cosmetic manufacturer.
Key Specifications
R&D Laboratory
Our R&D laboratory is where your formula is born. Staffed by qualified cosmetic chemists with active ingredient expertise — PDRN, peptides, barrier actives, Vitamin C derivatives, botanical extracts. Every formula goes through internal stability and compatibility testing before dispatch as a sample. We do not send unstable formulas. We do not guess.
Key Specifications
10 Production Lines
Ten dedicated filling and assembly lines handle every product category — from precision ampoule filling to high-speed sheet mask sealing. Inline quality checks are performed at every production station. Batch production records — raw material usage, filling parameters, operator records — are maintained for every order and available for audit.
Key Specifications
Quality Control Laboratory
Our QC laboratory tests every production batch before release — not just at random intervals, and not just visually. pH, viscosity, microbiological testing, heavy metals, and stability are confirmed against the approved specification. A Certificate of Analysis (COA) is issued for every batch. This is what your buyers and regulators will ask for — and we have it, documented, for every order.
Key Specifications
Packaging & Warehouse
From label application to final carton, our packaging area operates with inline quality checks at every step. Every unit is scanned, inspected, and verified before being packed into outer cartons. The raw materials warehouse operates with strict Incoming Quality Control — every ingredient is tested against its COA and SDS before being approved for production.
Key Specifications
VIRTUAL AUDIT
Arrange a Live Virtual Factory Audit
We welcome virtual audits via video call. A typical audit covers: live facility walkthrough, QC documentation review, COA and GMP certificate verification, and a Q&A with our production and QC managers. Most audits take 30–45 minutes.
Physical visits also welcome — contact us to arrange in advance.