Formulation & SKU Selection
Choose from nine ODM lines or develop a custom formula with our specialists and partner labs.
How We Work: Your OEM & ODM Journey from Idea to Shelf
Transparent, collaborative process — you work with us; we orchestrate partners, compliance, and delivery.
Understanding Your Options
ODM (Original Design Manufacturing)
Leverage our formulation portfolio and supply chain team for turnkey OEM & ODM — concept to shelf with one contract, one contact.
- Nine ready-to-label ODM lines across deodorant, grooming, and oral care
- Production at FDA-registered partner facilities with GMP compliance coordinated by our team
- Comprehensive regulatory documentation for global markets (FDA, EU REACH, APAC)
- Customizable packaging solutions with eco-friendly options
- Flexible MOQ starting from just 1,000 units
- Dedicated account management and technical support
Ideal for: New brands, e-commerce startups, retailers launching private labels, and entrepreneurs seeking rapid market entry with minimal R&D investment.
OEM (Original Equipment Manufacturing)
Bring your proprietary formula to life through partner-facility OEM production under our QC and documentation management.
- OEM production of your formulations at qualified partner lines with exact specifications
- Advanced production capabilities with batch traceability
- Rigorous quality control protocols and stability testing
- Regulatory compliance support and documentation preparation
- Scalable production volumes with MOQ from 5,000 units
- Confidentiality agreements and IP protection
Ideal for: Established brands with existing formulations, companies with specific ingredient requirements, and businesses seeking an accountable OEM & ODM partner who manages OEM production and export documentation.
Deodorant SpraysGrooming & CleansingOral Care
How We Orchestrate Your Supply Chain
You sign with Pu Yan. We coordinate formulation partners, qualified production sites, QC, compliance documentation, and export logistics — so you are not juggling five suppliers.
Partner-Facility Production
Manufacturing at vetted GMP-aligned facilities with IQC, IPQC, OQC, and optional third-party inspection.
Compliance & Documentation
SDS, COA, stability data, and market-specific dossiers aligned to your target regions.
Export & Delivery
FOB, CIF, or DDP coordination with batch traceability from production to customs-ready shipment.
Supplier Qualification Hub
Standard answers and checklists procurement teams use before signing an integrated OEM & ODM supply chain partner.
ODM vs OEM: Which Model Fits Your Brand?
Compare service scope, IP ownership, and typical commercial terms at a glance.
| Feature | ODM | OEM |
|---|---|---|
| Formula source | Our proven or custom-developed formulas | Your proprietary formula |
| Formula IP | Licensed / shared per agreement | Your full IP ownership |
| Typical MOQ | From 1,000 units | From 5,000 units |
| Sample lead time | 7–10 business days | 2–3 weeks (formula validation) |
| Regulatory documentation | Full export dossier included | Compliance support for your formula |
| Packaging customization | Private label & retail-ready options | Per your specifications |
| Best for | New brands & rapid market entry | Established brands with own R&D |
Our Collaborative Process
Six structured phases guiding your product from initial consultation to global delivery.
01
Step 1
Strategic Consultation & Discovery
We begin with an in-depth consultation to understand your brand vision, target market demographics, competitive landscape, and specific product requirements. This foundational phase ensures we align our approach with your business objectives and customer needs.
02
Step 2
Formula Selection & Customization
Based on your requirements, we present proven formulations from our portfolio or develop custom solutions with our formulation specialists and partner labs. We provide detailed ingredient analysis, safety assessments, and performance data to support your decision-making process.
03
Step 3
Prototype Development & Testing
We coordinate prototype samples from partner facilities for your evaluation, typically delivered within 7-10 business days. We conduct preliminary efficacy and stability testing to ensure the formulation meets performance standards before proceeding to full-scale production.
04
Step 4
Comprehensive Validation & Compliance
We perform rigorous testing protocols including stability studies, microbial challenge testing, and safety assessments. Simultaneously, we prepare all necessary regulatory documentation for your target markets, ensuring full compliance with FDA, EU, and other regional requirements.
05
Step 5
Regulatory Documentation & Approvals
Our regulatory experts compile comprehensive dossiers including Safety Data Sheets (SDS), Certificates of Analysis, and compliance certificates. We guide you through any required registration processes and maintain ongoing regulatory monitoring for your markets.
06
Step 6
Production Coordination & Global Delivery
Through qualified GMP-certified partner facilities, we execute production with QC at every stage. Our logistics team ensures reliable delivery to your specified locations worldwide, with real-time tracking and inventory management support.
Typical Timeline
Estimated durations for a standard OEM & ODM project — timelines may vary based on customization level.
1-2 weeks
Strategic Consultation & Discovery
Phase 12-4 weeks
Formula Selection & Customization
Phase 22-3 weeks
Comprehensive Validation & Compliance
Phase 34-6 weeks
Production Coordination & Global Delivery
Phase 4Total project timeline is typically 10–15 weeks from consultation to delivery.
Quality Control & Inspection
Multi-stage QC managed across our supply chain — from raw material intake to pre-shipment inspection. Third-party inspection welcome.
01
Incoming Material QC (IQC)
Raw materials verified against specifications, COA, and supplier audit records before entering production.
02
In-Process QC (IPQC)
Batch monitoring during mixing, filling, and packaging with inline weight, volume, and appearance checks.
03
Finished Goods QC (OQC)
Final inspection against AQL standards covering labeling, seal integrity, fill level, and packaging compliance.
04
Third-Party Inspection
SGS, Intertek, or buyer-nominated inspection agencies supported before shipment upon request.
Ready to Start Your OEM & ODM Journey?
Contact us today to schedule your initial consultation.
Get Started