CELLAB Co., Ltd.

Q.01 What is the Minimum Order Quantity (MOQ) to begin production?

CELLAB operates flexible multi-item small-batch lines alongside high-capacity equipment. Depending on the product category and packaging type, we support flexible production starting from 1,000 to 3,000 units. We propose optimal production strategies to minimize inventory risks for startups and growing indie brands.

Q.02 How long does the lead time take from initial planning to final delivery?

When utilizing CELLAB's verified standard formulations, production is completed within approximately 3 to 4 weeks. For customized new formula research and customized packaging manufacturing (printing, mold tooling, etc.), it typically takes 6 to 8 weeks. Fast-track production schedules aligned with urgent launch dates are actively supported.

Q.03 What is the procedure for formulation sampling, and are there sampling fees?

Following development consultation, initial prototype formulation samples are prepared and dispatched free of charge. After evaluating the initial sample, feedback regarding absorption, oil/moisture balance, scent, and texture is incorporated through 2nd and 3rd round modifications until the client is 100% satisfied.

Q.04 Do you provide one-stop support for container sourcing and packaging artwork?

Yes. We have a dedicated in-house design and packaging procurement team. Through extensive partnerships with domestic and global container manufacturers, we provide end-to-end (turn-key) solutions from container and carton sourcing to labeling artwork and cosmetic regulatory compliance review.

Q.05 Can you assist with functional cosmetic regulatory filings and clinical efficacy testing?

CELLAB's Regulatory Affairs Team handles official MFDS functional cosmetics filings (brightening, wrinkle care, UV protection, anti-hair loss). Furthermore, we partner with accredited clinical testing institutes to coordinate human hypoallergenic patch tests, 24-hour hydration retention, and lifting efficacy trials at preferred partnership rates.

Q.06 Can you issue international export regulatory documents such as FDA, CPNP, and NMPA?

CELLAB Co., Ltd. is a global cosmetic manufacturer certified with MFDS CGMP and international ISO 22716. We issue all necessary export documentation, including Certificate of Free Sale (CFS), Certificate of Analysis (COA), Material Safety Data Sheet (MSDS), full quantitative ingredient formulas, and manufacturing process flowcharts.

Q.07 Can our brand utilize CELLAB's patented bio-ingredients and specialized formulations?

Absolutely. You can leverage CELLAB's exclusive intellectual property—such as our US-patented activated charcoal nano-dispersion technology, fermented Lotus Corniculatus bio-extract, herbal anti-inflammatory complexes, and temperature-responsive hydrogels. Official patent numbers can be printed on packaging for powerful brand differentiation.

Q.08 Can clients supply their own specific raw materials or packaging components?

Yes. Clients may provide proprietary patented extracts, designated containers, or specialized secondary packaging for OEM toll manufacturing at CELLAB's facilities. Supplied materials undergo quality and safety verification in accordance with MFDS cosmetic regulations and CGMP standards.

Frequently Asked Questions (FAQ)