COSMETIC GMP MANUFACTURING
Every ORALABX project runs on the same documented sequence — briefing, formulation, packaging, sampling, testing, production. This page shows what happens at each stage, what we need from you, and how long it takes.
From formulation briefing to bulk production, every step is documented, validated, and aligned with global regulatory standards. Designed for scalable private-label oral-care manufacturing.
From approved product brief to batch release, our documented workflow supports commercial production, compliance review, and supply planning.
Share your brand goals, target markets, product formats, and functional requirements.
We start from your destination market, product category, positioning and claim direction. That determines which formulation routes are open to you and which documentation set your importer will need — both are cheaper to settle now than after sampling.
Develop stable, compliant formulations tailored to your product vision.
Formulation work is carried out with the R&D team at our long-term partner manufacturing base, working either from an existing stable base or from your own specification. Raw materials are sourced from qualified suppliers with traceable documentation.
Select packaging formats optimized for function, branding, and logistics.
Bottles, tubes and spray systems are selected for material compatibility, filling stability and shipping economics. Stock tooling ships on the standard timeline; custom tooling is possible but adds significantly to it — see the timeline below.
Evaluate production-standard samples before commercial production.
Production-standard samples are prepared for technical evaluation against the approved product brief. Refinement is limited to the agreed development scope before formula approval and commercial production.
Comprehensive testing and regulatory validation.
Final-product stability testing runs 90–180 days in the factory lab. Third-party testing is commissioned from ISO 17025-accredited laboratories (SGS, BV, Intertek) according to your market: preservative efficacy, microbial limits, heavy metals and packaging migration. We supply the manufacturing-side data your Responsible Person or importer needs; market registration itself remains with your local entity.
ISO/GMP manufacturing with full batch traceability.
Production runs at our long-term partner manufacturing bases in Fujian, China, operating under ISO 9001 and cosmetic GMP (ISO 22716) systems with batch-level records. Each batch is released against specification before shipment. We coordinate export documentation and delivery to your port or facility.
A clear division of responsibility prevents delays around FSC, registration, labeling, testing and destination-market documentation.
Formula and product development, manufacturing, quality control, batch documentation, and agreed manufacturing-side technical documents.
Local registration, import licence, market authorization, claims approval, authority submission, and final local regulatory responsibility.
Artwork, market-specific labeling, testing scope, and shipping or documentation coordination.
Document availability, legalization, third-party testing and destination-market services are confirmed and quoted by project—not assumed as default.
Our standard is 10,000 units per SKU. We publish the real production window rather than a best case, so that your launch date holds.
1-2 days
5-7 days
3-5 days
45–60 calendar days
5–7 days (air) / 25–40 days (sea)
Send us your product concept, target market and volume. We will tell you what is feasible and what it will take.
