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postmaster@laeyolabs.com广州市花都区花山镇华辉路18号
微观化妆品创意产业园E栋整栋Company
Guangzhou Laeyo Biotechnology Co., Ltd., founded in 2015, is a modern high-tech beauty manufacturer specializing in full-service cosmetic OEM/ODM. We support customized production across cosmetic filings, hygiene product filings, and medical device registrations, enabling distribution through hospitals and pharmacies. Our capabilities cover professional salon lines, mass-market personal care, and specialty retail chains.
Laeyo operates two R&D centers, including an 8,000㎡ biotechnology R&D facility with a central lab, botanical extraction lab, physical & chemical testing lab, microbiological challenge room, efficacy testing lab, and product experience lab. Our team brings together experts across chemistry, biology, traditional Chinese medicine, and nutrition science.
We also run a 10,000㎡ manufacturing base built to international GMPC standards and certified to EU ISO 22716, featuring Class 100,000 GMP workshops, aseptic automated filling rooms, an ultrapure water system, and 50+ automated production lines. Our operation is supported by nearly 500 production professionals and a 30-person R&D team, including PhD-level specialists.
Empowering your brand with our top OEM/ODM cosmetic solutions.
Mission: Build quality through integrity, lead with innovation, and be the OEM partner brands trust most.
We prefer proof over promises—documents, test plans, traceability and real process visibility.
Sampling, packaging-fit, and timeline are managed as one integrated system.
We align documentation and claims boundaries by your target market and channel.
For over a decade, we’ve specialized in OEM cosmetics manufacturing. Each year, our factory produces more than 100 million skincare units shipped to customers across markets worldwide.
Over the past few years, we’ve supported well-known brands worldwide. With advanced capabilities and strict quality control, we produce high-quality products that help you grow your brand and improve profitability.
Our manufacturing workflow is designed around GMPC discipline—raw material QC, controlled production, filling, packaging, and finished goods release.
A practical sampling loop built for fast launches: direction → samples → 1–2 iterations → production alignment.
We support both “ready formula with brand” and “custom formulation + packaging” routes. Most buyers move faster when they confirm target market, claims direction, and packaging early.
Typical sampling expectation: initial samples in 3–7 days (depending on brief and packaging plan), then 1–2 iteration rounds for sensorial, fragrance, and claims boundary alignment.
What procurement teams usually request: stability, micro, compatibility, and market-facing documentation planning.
“GMP” is not just a certificate. Buyers typically need repeatable systems: batch records, traceability, and clear release criteria. We plan documentation and testing around your target market and channel.
For audit-ready proof, use the Trust Center to request the exact files you need (certifications, compliance documents, test reports, process evidence).
One place to verify: certifications, compliance files, factory proof, and IP documentation.
Third-party certifications and audit-ready proof for procurement teams.
Regulatory files and market-facing documentation you can request.
Patents and IP-related evidence for product differentiation and protection.
CONTACT US TODAY All of your questions will be answered by our team in a very quick/effective way