02 · MANUFACTURING
Qianlin Group connects production bases, clean environments, equipment and quality management to support medical devices, efficacy skincare and bio-based ingredients.
01 / PRODUCTION BASES
From the main production base to medical device and color cosmetics facilities, Qianlin Group uses a regional manufacturing network to support different product directions. Select a map hotspot or base name to explore.
01 / GUANGDONG QIANLIN
With a floor area of 35,000 m² and current investment of RMB 150 million, the base has annual capacity of more than 300 million units. It covers efficacy skincare, daily care and bio-based chemical ingredients, including planned capacity for patented ingredients, sheet masks, efficacy skincare and color cosmetics.
02 / YUNFU NOSAI
The base includes a 100,000-class GMP purification workshop and a sterile laboratory. Annual capacity exceeds 30 million units, covering medical masks, medical liquid dressings and medical water-light care.
03 / HUNAN MUTA
Located in central Hunan, the base holds 27 medical device registrations covering protective clothing, collagen dressings, medical steam eye masks and mussel adhesive protein dressings.
04 / KEBIER COSMETICS
A color cosmetics manufacturing facility focused on OEM lipstick, lip tint, brow pencils, eyeshadow and other categories. Products reach Europe, Southeast Asia and the Middle East.
02 / PRODUCTION EQUIPMENT
Production and inspection follow managed workflows, with equipment configured for product type, process and project scale.
03 / CLEAN WORKSHOPS
The manufacturing system covers medical devices, efficacy skincare and bio-based chemical ingredients, supporting development transfer and scaled production.
Workshop operation and environmental monitoring follow the requirements applicable to each product and process.
04 / QUALITY MANAGEMENT
Qianlin Group presents quality-system records and QC practices through compact image-and-text evidence modules.
The certificate records the quality-management basis and states validity through 16 October 2028.
Based on the 2022 Cosmetic Good Manufacturing Practice guidelines; the stated validity runs through 16 October 2028.
Covers incoming inspection, in-process monitoring, microbiological and physicochemical testing, finished-product inspection and batch traceability.
05 / GLOBAL SUPPLY CHAIN
06 / FACILITY REGISTRATION
FACILITY REGISTRATION
The document identifies the registrant and listed brand and states a validity period from 18 November 2025 to 17 November 2027.
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