CE Certified Medical Bodycare Manufacturer & Factory

Pioneering Clinical-Grade Formulations, Advanced Bio-Science Synthesis, and Resilient Global Supply Solutions for Leading Medical and Aesthetics Brands.

Corporate Profile & Manufacturing Capability

Discover Guangdong Miura Beauty Co. Ltd., a powerhouse of cosmetic science and medical-grade manufacturing excellence.

Guangdong Miura Beauty Co. Ltd.

We are a full-service cosmetics manufacturer specializing in high-performance OEM, ODM, and OBM solutions for global skincare and personal care brands. Based in Guangdong, China, we seamlessly combine advanced formulation science, modern automated production systems, and integrated brand development services to support our global clients from raw concept realization to retail-ready finished products.

Our Mission

To deliver safe, effective, and innovative skincare solutions through advanced manufacturing and scientific formulation—helping global beauty and medical brands develop faster, scale efficiently, and achieve sustained success in highly competitive, compliance-driven global markets.

Scale & Facilities

Our state-of-the-art 25,000-square-meter manufacturing facility is strictly regulated and fully equipped with 32 automated production lines. This massive operational capability enables high-efficiency, large-scale output while strictly maintaining the zero-tolerance quality control parameters required for premium and medical-grade products.

25k ㎡
Production Facility
32
Automated Lines
100%
GMP & ISO Compliant
R&D
Led by Formulation Chemists

Meet Our Expert Team

Our multidisciplinary team of scientists, regulatory experts, and engineers are the backbone of our CE-certified medical bodycare operations.

R&D & Formulation Team

🧪 Develops customized skincare solutions with optimized texture, stability, and performance based on global market trends and advanced cellular biology research.

Quality Assurance Team

🛡️ Ensures every product meets strict international standards through full-process testing and compliance control (GMP, ISO 22716, FDA, and CE MDR guidelines).

Packaging & Design Team

🎨 Creates complete brand packaging solutions, combining aesthetics, ergonomic functionality, sustainability requirements, and clear regulatory labeling.

Project Management Team

🌐 Provides end-to-end dedicated support for global clients, ensuring smooth bilingual communication, fast developmental cycles, and highly efficient logistics.

Traceable Manufacturing & Process Visuals

A look inside our GMP-compliant cleanrooms and automated machinery showcasing rigorous phase-by-phase quality assurance.

Raw Materials Control Area
Raw Materials Control
Vacuum Emulsifying Process
Emulsifying System
Material Standing & Aging Stage
Standing & Maturation
Automatic Filling Station
Automated Filling
Sterile Packaging Unit
Secondary Packaging
Smart Logistic Warehouse
Smart Warehouse Logstics
Stainless Steel Emulsifying Pot
Emulsifying Pot Assembly
Ultrasonic Bottle Washing Machine
Bottle Washing Station
Tail Sealing & Filling Machine
Tail Sealing & Tube Filling
Multi-track Liquid Filling Line
High-Speed Filling Lines
Smart Outer Packaging Wrapper
Advanced Packaging Machine

1. Regulatory Compliance & The Import of CE Certification

Within the modern cosmeceutical and medical aesthetics landscape, the margin between general skincare and medical-grade topical formulations is governed by rigid regulatory parameters. At Guangdong Miura Beauty Co. Ltd., our compliance framework is structured around Regulation (EU) 2017/745 (MDR) and global cosmetic directives, ensuring all products carrying our medical-grade label are certified for sale and professional use within the European Economic Area (EEA) and beyond.

CE certification is not merely a label; it represents verified clinical safety, biocompatibility, and batch-to-batch consistency. Our factory operates under strict ISO 13485 (Medical Devices - Quality Management Systems) standards, validating that every stage of our production—from raw material synthesis to vacuum emulsification and filling—meets the requirements of Class I and Class II medical-grade topicals.

"By integrating strict toxicology risk assessments, in-depth biocompatibility testing (ISO 10993), and verified clinical trials, we provide our global B2B clients with the legal and safety foundation required to scale their product portfolios without encountering regulatory hurdles."

2. Technical Formulation Roadmap & Bio-Science Innovations

The progression of medical bodycare lies in targeted delivery systems and advanced bio-active agents. Our R&D team works at the interface of dermatological science and cellular repair. The formulation roadmap below outlines our core focus zones designed to maximize transdermal efficacy:

Advanced Peptide & PDRN Synthesis

Harnessing the regenerative power of Polydeoxyribonucleotide (PDRN) and GHK-Cu (Copper Peptide) complexes to stimulate cellular renewal, promote collagen synthesis, and accelerate healing in post-procedure skin.

Double-Layer Nano-Encapsulation Delivery

Stabilizing volatile actives (such as Pure Vitamin C, Retinol, and Peptide compounds) inside nano-liposomes. This controls transdermal penetration, facilitating targeted release within deep epidermal layers while preventing skin irritation.

Skin Barrier Biomimicry

Replicating the natural intercellular lipids (ceramides, cholesterol, and free fatty acids) in precise ratios. This technology mimics the skin’s structure, instantly reinforcing damaged skin barriers following clinical treatments.

Furthermore, our deep exploration of bio-active extracts—including specialized snail mucin filtrates, centella asiatica isolates (such as madecassoside), and biotechnologically derived hyaluronic acid—allows us to manufacture lightweight gels, rich creams, and concentrated serums that exhibit exceptional stability profiles and high skin tolerance.

3. Macro Industry Solutions: From Clinical Post-Care to Daily Prevention

Modern consumers demand results that bridge the gap between clinical treatments and daily home care. Our OEM/ODM solutions are tailored to meet these macroeconomic demands. We segment our production capability into specialized treatment classes:

Product Category Key Biological Actives Target Treatment Indications Compliance Standard
Clinical Post-Procedure Care PDRN, Copper Peptides, Centella Calming Ampoules Post-Laser, Microneedling, and RF Treatment Recovery CE MDR Class I, ISO 13485
Dermatological Anti-Aging Encapsulated Retinoids, Snail Mucin, Niacinamide Fine Lines, Skin Laxity, and Deep Hydration Support ISO 22716, GMPC
Hyperpigmentation Correction 3-O-Ethyl Ascorbic Acid, Salicylic Acid, Kojic Acid Melasma, Dark Spots, and Post-inflammatory Hyperpigmentation GMPC Compliant
Pediatric & Hypoallergenic Organic Shea Butter, Colloidal Oatmeal, Ceramides Atopic Dermatitis, Dry/Sensitive Infant Skin Care Hypoallergenic Certified

4. China Factory 4.0: Supply Chain Resilience & Automation

As a leading Chinese manufacturer located in the industrial manufacturing hub of Guangdong, Guangdong Miura Beauty Co. Ltd. represents the peak of Factory 4.0 automation. Our 25,000 m² facility is highly integrated, allowing us to leverage automated systems to maintain cost advantages, minimize human error, and guarantee consistent product safety.

Our infrastructure includes:

  • Automated Emulsification Pods: Vacuum homogenizers featuring precise temperature profiles and shear rates to guarantee highly stable emulsion formations.
  • High-Speed Automated Filling Lines: Capable of handling diverse container profiles from clinical ampoules and airless pump bottles to flexible tubes under strict cleanroom conditions.
  • Digitized Inventory & Batch Tracking: End-to-end ERP systems monitoring raw materials from source to final distribution, offering 100% trace-back capabilities.

By optimizing our localized raw material supply networks, we offer global clients insulation from supply chain shocks, reduced production lead times, and predictable container transport shipping pipelines.

5. Global B2B Procurement Framework: OEM, ODM & OBM

We work with brand owners, clinic chains, and global distributors to provide clear, low-risk procurement pipelines. Our service packages are divided into three distinct avenues:

OEM (Original Equipment Manufacturing)

Clients provide pre-approved formulations and packaging specifications. We handle large-scale manufacturing, quality control, packaging compliance, and logistical execution.

ODM (Original Design Manufacturing)

Our R&D team provides ready-to-market formulations. Clients select customized scents, active ingredients, and outer packaging profiles to align with their brand identity.

OBM (Original Brand Manufacturing)

Complete product concepts, including clinical studies, packaging design, legal registration support, and retail display strategies, ready for immediate global deployment.

6. Localization Support, Registration Assistance, & Compliance Auditing

Navigating global border control and domestic cosmetic registration can be challenging. Our specialized project management and regulatory team provides active assistance to streamline these processes. We offer complete technical documentation, including:

  • Product Information Files (PIF) for EU markets.
  • Safety Data Sheets (SDS) and Certificates of Analysis (COA) for every batch.
  • FDA cosmetic registration dossiers and stability reports.
  • Assistance with local CPNP (Cosmetic Products Notification Portal) notifications.

We regularly host third-party verification auditors from SGS, Intertek, and various international regulatory bodies. Our facility maintains a transparent, open-book audit policy to ensure our partners remain confident in our standards.

Technical Q&A / FAQ

Expert insights on regulatory compliances, manufacturing capability, and OEM partnership processes.

What defines a "CE Certified" bodycare product compared to a regular cosmetic?
CE certified medical bodycare products comply with the European Union's medical device regulations (MDR 2017/745). They are formulated to address physiological conditions (such as damaged skin barriers, post-surgical wounds, or severe dermatitis) and undergo stringent biocompatibility, cytotoxicity, and clinical trials to ensure their medical efficacy and safety, whereas standard cosmetics are intended for basic cleaning, perfuming, or changing appearance.
Does Guangdong Miura Beauty Co. Ltd. support custom formula development (ODM)?
Yes, we feature a fully staffed laboratory led by cosmetic chemists and formulation scientists. We can take benchmark samples, refine textures, integrate specific active components (such as PDRN, copper peptides, or customized botanical extracts), and design stable formulas from scratch.
What certifications does your factory hold?
Our 25,000-square-meter facility operates under ISO 22716 (Good Manufacturing Practices for Cosmetics), GMPC (US & Europe guidelines), and ISO 13485 (Medical Devices Quality Management Systems) standards.
How does your quality assurance team verify batch consistency?
Every batch undergoes physical, chemical, and microbiological testing (viscosity, pH, active ingredient assay, stability monitoring, and heavy metal limits). We provide a detailed Certificate of Analysis (COA) for every shipment before leaving our facility.
What are the Minimum Order Quantities (MOQs) for OEM/ODM orders?
Our MOQs depend on the packaging format and formulation complexity. Generally, for standard creams, gels, and serums, MOQs start at 5,000 units. Customized medical-grade ampoules or custom-shaped tubes may require higher MOQs depending on raw material sourcing.