✓ ISO 22716 & GMPC Certified ✓ 20,000㎡ Facility · 500K Daily Capacity ✓ Flexible MOQ & Custom Solutions ✓ Free Sample Available · 24H Quick Quote

Best Selling Formulas

Market-validated skincare formulations trusted by 1,000+ global brands across 100+ countries. ISO 22716:2007 & GMPC certified manufacturing with flexible MOQ.

OEM / ODM Service Process

A structured 5-stage workflow — from initial brief to door-to-door delivery. Every stage follows ISO 22716:2007 GMP quality system requirements.

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Product Brief & Formula Matching

Share your brand vision, target market, and requirements. Our R&D team screens 10,000+ stability-tested base formulas or initiates a custom development brief using DOE (Design of Experiments) methodology. Recommended formula matches delivered within 2 business days.

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Lab Sampling & Stability Testing

3–5 complimentary 100g lab-scale samples prepared and shipped via DHL/FedEx within 7–10 business days. Concurrently, accelerated stability testing is conducted at 40°C ± 2°C / 75% ± 5% RH (3-month protocol) with pH, viscosity, and organoleptic monitoring at T0, T15, T30, T60, and T90 checkpoints.

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Packaging Engineering & Artwork

Select from 200+ stock container options (airless pumps, laminated tubes, PCR bottles, glass jars) or commission custom mold development. Die-line templates provided within 3 days. In-house design team finalizes artwork to your brand guidelines with Pantone color matching.

Pilot Batch & Full-Scale Production

Pilot batches produced for final sign-off. Full-scale mass production runs across 12 automated GMPC cleanroom lines: vacuum emulsification (3,000L capacity), gravimetric servo filling (±0.5% accuracy), torque-controlled capping, and in-line weight check. Microbiological testing per ISO 11930 at each batch.

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Quality Release & Global Logistics

Final QC panel: organoleptic evaluation, USP <61>/<62> microbial limits, packaging integrity (seal strength, drop test), and full batch record review with electronic signature sign-off. Shipment via FOB, CIF, or DDP terms. Documentation package: COA, MSDS (GHS Rev.8), BSE/TSE, allergen declaration, certificate of origin.

Our Advantages & Certifications

Independently audited manufacturing. 20+ years of documented quality performance (Est. 2004) serving 1,000+ brands across 100+ export markets.

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ISO 22716:2007 GMPC Certified

Facility independently audited to ISO 22716:2007 Cosmetic GMP guidelines. Full batch traceability via ERP — every ingredient lot, equipment CIP/SIP log, environmental monitoring record, and QC data point is digitally captured and retrievable for the product's entire lifecycle.

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20,000m² Manufacturing Base

Intelligent production facility equipped with 12 automated production lines, vacuum emulsifiers (300–3,000L capacity), and high-speed robotic packing systems. Daily output reaches 500,000 finished units with strict cleanroom quality assurance.

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Flexible MOQ & Scalable Production

Tailored batch structures to support emerging indie labels and multinational brands alike. Agile test runs with seamless scaling into full-volume production runs without compromising lead times or formulation integrity.

20+ Years · 1,000+ Brands · 100+ Markets

Founded in 2004, backed by 1,000+ team specialists and 100+ patents. Reliable global export capability compliant with US FDA MoCRA, EU EC No. 1223/2009, ASEAN Cosmetic Directive, GCC, and Halal standards across 100+ countries.

B2B Frequently Asked Questions

Technical and commercial answers for brand owners evaluating our OEM/ODM services.

Our sample workflow has three stages. Stage 1 — Formula Selection: within 2 business days of receiving your brief (target market, price point, product claims, texture preference), we recommend 3–5 matched base formulas from our 10,000+ library. Stage 2 — Lab Sampling: selected formulas are prepared as 100g lab batches and shipped via DHL/FedEx/UPS within 7–10 business days. Stage 3 — Stability Validation: concurrent accelerated stability testing is conducted at 40°C/75%RH, 25°C/60%RH, and 4°C conditions for 90 days. Data is delivered as a comprehensive stability report covering pH, viscosity, specific gravity, organoleptic evaluation, and microbial challenge testing (ISO 11930). In-stock reference library samples ship in 3–5 days.
Yes. Our R&D laboratory is supported by 100+ patents and over 1,000 dedicated professionals, operating a structured 6-phase development workflow: Competitive Benchmarking, Ingredient Sourcing, DOE Prototyping, 12-week Accelerated Stability Testing, Consumer Sensory Panels, and Scale-up Pilot Production. Full IP ownership of custom formulas transfers to your brand upon project completion.
We provide a complete documentation package tailored to your target market across 100+ export destinations. Standard documents include: Certificate of Analysis (COA) with full physical/chemical specifications and heavy metals testing (USP <232>/<233>), GHS Rev.8-compliant MSDS/SDS, Technical Data Sheets (TDS), IFRA certificates, allergen declarations, and non-animal testing statements. For EU markets: CPSR dossier components and PIF documentation. For US markets: FDA MoCRA facility registration and listing compliance documents.

Ready to Launch Your Skincare Brand?

Send us your product brief. Receive free samples, a tailored OEM/ODM proposal, and a project timeline — NDA-protected, response within 24 hours.

Request Free Quote & Samples