Leadership & Science Team
Experienced cosmetic scientists, formulation experts, and manufacturing leaders behind our skincare OEM/ODM solutions.
- Cosmetic Chemists & Formulation Scientists
- GMP Manufacturing Leadership
- R&D-Driven Skincare Development
- Global Regulatory Experience (EU / US)
Our Approach
Every formulation decision is guided by scientific rigor, not marketing trends. Our methodology is built on five foundational principles that define how we develop every product.
Science-Led Formulation
Every formula begins with ingredient mechanism research — not trend-chasing. We study active ingredient penetration, stability, and compatibility before proposing any formulation path.
Safety-First Development
Preservative efficacy, microbial limits, and dermal compatibility are validated at lab scale before any pilot production begins. Safety is never an afterthought.
Regulatory Compliance Mindset
EU CPNP, FDA MoCRA, and ASEAN cosmetic directive requirements are embedded from the first ingredient selection — not retrofitted before export.
Active Ingredient Innovation
Continuous research into encapsulated retinol, biomimetic peptides, stabilized vitamin C, and microbiome-friendly preservatives keeps our formulation library ahead of market shifts.
Evidence-Based Product Design
Claims are supported by stability data, in-vitro testing, and ingredient-level efficacy research. We build the data package before the marketing message.
Leadership Team
Decades of combined experience in cosmetic manufacturing, quality assurance, and international regulatory affairs.
MR Zhao
CEO & Founder- 22+ years in cosmetic manufacturing and international trade
- Led company growth from startup to 1,000+ brand partnerships
- Established export channels to 30+ countries across EU, US, and APAC
- Strategic direction for GMP facility investment and R&D expansion
Leo
Head of Manufacturing- 18 years in GMP pharmaceutical and cosmetic production management
- Oversaw commissioning of 8 automated production lines and ISO Class 7 cleanroom
- Scaled monthly output from 500,000 to 1.5 million units
- Certified in GMP, ISO 22716, and Lean Manufacturing methodologies
Daisy
Head of Quality Assurance- 15 years in cosmetic and OTC pharmaceutical quality management
- Designed and implemented the 3-stage QC system (IQC / IPQC / OQC)
- Led successful ISO 22716 and COSMOS Organic certification audits
- Manages a team of 12 QC analysts and 4 microbiology technicians
Cathy
Head of Regulatory Affairs- 12 years in global cosmetic regulatory compliance
- Deep expertise in EU CPNP, FDA MoCRA, and ASEAN cosmetic directive requirements
- Manages PIF documentation and safety assessment coordination for all export markets
- Led FDA OTC drug establishment registration and facility listing
Scientific Team
The core of our OEM/ODM capability — our in-house scientific team transforms brand concepts into safe, stable, and commercially viable skincare formulations.
Cosmetic Chemists
- Formulation Development — Design and optimize O/W and W/O emulsions, serums, gels, and anhydrous systems tailored to client specifications
- Ingredient Compatibility Research — Analyze active ingredient interactions, pH optimization, and preservation system selection for each unique formula
- Stability Optimization — Conduct accelerated and real-time stability studies, adjusting formulations based on data to meet 24-36 month shelf-life targets
- Texture & Sensory Design — Fine-tune spreadability, absorption rate, and after-feel using rheology modifiers and emollient systems
R&D Scientists
- Active Ingredient Research — Evaluate novel actives including encapsulated retinol, biomimetic peptides, growth factors, and botanical extracts for efficacy and formulation compatibility
- Skin Biology Understanding — Apply knowledge of epidermal barrier function, melanogenesis pathways, and dermal matrix biology to design targeted treatment formulations
- Product Innovation Pipeline — Maintain a forward-looking innovation calendar tracking emerging ingredient technologies, delivery systems, and clean beauty preservation methods
Lab Technicians
- Testing Execution — Perform microbial limit testing, preservative efficacy challenge tests (ISO 11930), and pH/viscosity measurements with full documentation
- Stability & Safety Tests — Operate accelerated stability chambers and conduct freeze-thaw cycling, centrifugation stress tests, and photostability assessment
- Sample Validation — Prepare and validate lab-scale samples for client evaluation with precise batch documentation ensuring formula reproducibility at production scale
Expertise & Credentials
Academic Background
- Advanced degrees in Cosmetic Science, Chemistry, Biochemistry, and Chemical Engineering
- Specialized training in emulsion science, surfactant chemistry, and polymer rheology
- Continuing education in dermatological formulation safety and skin physiology
Industry Certifications
- GMP for Cosmetics — ISO 22716 internal auditor certified
- HACCP-certified quality management professionals
- Certified Cosmetic Safety Assessor training (EU Regulation 1223/2009)
- FDA 21 CFR Part 210/211 cGMP training for OTC drug products
Technical Proficiencies
- HPLC analysis for active ingredient quantification and stability monitoring
- FTIR spectroscopy for raw material identity verification
- Rheology and texture analysis for sensory profile optimization
- Microbiological testing per ISO 21149, ISO 22718, and pharmacopoeia methods
R&D Process & Methodology
We are a research-driven development organization — not a contract filler. Our formulation process follows a structured, data-driven pipeline designed to de-risk product development for our clients.
Ingredient Research
Literature review, supplier qualification, and mechanism-of-action analysis for each active ingredient candidate. Regulatory screening for target markets conducted in parallel.
Formulation Design
Selection of emulsion system, thickener, preservative, and sensory modifiers. Computational modeling of ingredient interactions before bench work begins.
Testing & Validation
Accelerated stability (40°C/75% RH), freeze-thaw cycling, centrifugation stress testing, and preservative challenge. Only formulas passing all gates advance.
Optimization
Iterative refinement of texture, stability, and sensory profile based on quantitative data. pH and viscosity drift analyzed over time points to guarantee shelf-life performance.
Scaling Production
Pilot batch (50L) validated against lab-scale benchmarks. Process parameters locked. Full-scale production (500L-2,000L) with IPQC monitoring at every critical control point.
Data-Driven Formulation
Every decision — from emulsifier HLB selection to preservative concentration — is supported by quantitative stability data, not intuition.
Stability & Safety Validation
Multiple parallel stability protocols ensure that every formulation meets shelf-life targets before client delivery.
Market Trend Integration
Active tracking of ingredient trends — encapsulated retinol, multi-weight HA, biomimetic peptides, microbiome-friendly preservation — integrated into formulation recommendations.
Regulatory & Compliance Expertise
EU CPNP Compliance
Full capability to prepare and submit Cosmetic Product Notification Portal entries. Our regulatory team manages Responsible Person coordination, safety assessment documentation (CPSR), and product information file (PIF) preparation for EU market access.
FDA Labeling & Compliance
MoCRA-compliant facility registration and product listing support. INCI-compliant ingredient labeling, OTC drug monograph compliance (sunscreens, anti-acne, anti-dandruff), and 21 CFR Part 701 labeling review.
Ingredient Regulatory Screening
Pre-formulation screening of every ingredient against Annex II-VI of EU Regulation 1223/2009, FDA prohibited/restricted lists, and ASEAN Cosmetic Directive annexes to ensure multi-market compliance from day one.
Safety Documentation
Preparation of complete safety dossiers including CPSR (Cosmetic Product Safety Report), SDS (Safety Data Sheets), allergen disclosure statements, and Certificate of Analysis (COA) documentation for every production batch.
How We Collaborate with Clients
Our scientific team works as an extension of your brand — not a distant supplier. Every collaboration follows a structured, transparent process.
Formula Customization
Your concept, our science. We translate brand vision into a technical formulation brief, recommending ingredient systems that balance efficacy, stability, and cost targets.
Private Label Development
Start with 8,000+ existing base formulas. Modify texture, fragrance, actives, and packaging to create a differentiated product line under your brand name.
Brand Positioning Consultation
Our team advises on ingredient story, claims substantiation strategy, and regulatory positioning to align your product with target market expectations.
Sample Iteration Process
Lab samples delivered in 10-15 business days. Structured feedback loop: your sensory evaluation informs formula refinement until the product matches your vision exactly.
Innovation & Trend Research
Anti-Aging Skincare Trends
- Encapsulated retinoid systems with reduced irritation profiles
- Biomimetic peptides targeting specific collagen synthesis pathways
- Bakuchiol as a retinol alternative for sensitive skin formulations
- Multi-weight hyaluronic acid for multi-layer hydration
Clean Beauty Development
- COSMOS-compliant formulation development for organic certification
- Preservative systems free from parabens, formaldehyde donors, and MIT
- Vegan and cruelty-free formulation protocols
- Microbiome-friendly formulations preserving skin barrier integrity
Sensitive Skin Formulations
- Minimalist ingredient decks for atopic and reactive skin types
- Ceramide-dominant barrier repair formulations
- Fragrance-free and essential-oil-free options with sensory compensation
- Prebiotic and postbiotic ingredient integration for skin microbiome support
Active Ingredient Innovation
- Stabilized L-ascorbic acid systems (water-free and anhydrous suspensions)
- Liposomal delivery systems for enhanced active ingredient penetration
- Growth factor and exosome technology for advanced regenerative formulations
- Time-release actives for prolonged efficacy with reduced irritation
Our Working Environment
See where our formulations are developed, tested, and validated — a BSL-2 laboratory integrated within our GMP manufacturing facility.
Team Scale & Structure
Organizational Integration
R&D, QC, Regulatory, and Production teams operate as integrated, cross-functional units — not siloed departments. Formulation scientists work alongside production engineers during scale-up. QC analysts collaborate with R&D during stability protocol design. Regulatory specialists are embedded in the formulation review process from day one.
Our Commitment
Continuous Training
Quarterly training cycles on emerging ingredient technologies, regulatory updates (EU, FDA, ASEAN), and analytical method advancements. Every scientist completes 80+ hours of continuing education annually.
Knowledge Sharing
Internal technical seminars, cross-department formulation reviews, and a shared knowledge base of stability data, ingredient performance metrics, and regulatory intelligence accessible to all team members.
Commitment to Safety
Every team member — from formulation scientist to packaging technician — is trained in GMP principles and understands their role in maintaining product safety. Safety is not a department; it is a shared responsibility.