未分类

2025 China OEM Cosmetics Factory Cooperation Guide: 5 Practical Methods for 30% Cost Reduction + Zero Compliance Risk, with Contract Template

I. New Pain Points in China OEM Cosmetics Factory Cooperation (2025): Core Contradictions Revealed by 3 Sets of Data​

According to the Q3 2025 report from China Beauty Industry Research Institute, there are three prominent contradictions in the cooperation between brands and OEM factories, which are also high-frequency search issues:​

  1. Cost-Quality Imbalance: 68% of startup brands report that “quotations exceed budgets”, but 32% of them encounter substandard raw materials (e.g., industrial-grade glycerin replacing cosmetic-grade glycerin) after blindly choosing low-cost factories;​
  1. Compliance-Efficiency Conflict: After the implementation of the new Guidelines for the Submission of Cosmetic Raw Material Safety Information, 45% of factories experience raw material registration delays, prolonging order delivery cycles from 30 days to 45 days;​
  1. Inadequate Cross-Border Adaptation: Among brands exporting to Southeast Asia, 52% have faced customs clearance obstacles because factories failed to master the “prohibited ingredient list” in ASEAN’s Cosmetics Directive.​

II. “Cost-Compliance” Dual-Control System Under EETA Principles (Rare Practical Methods)​

(I) Experience-Oriented: 4 Non-Routine Techniques for 30% Cost Reduction (From 100+ Brand Cases)​

  1. Raw Material Group Procurement Collaboration: Unite 3-5 small brands in the same category to negotiate “joint raw material procurement” with factories. The procurement cost of core raw materials such as imported hyaluronic acid can be reduced by 15%-20% (a group procurement sharing agreement must be signed to clarify dosage and cost proportion);​
  1. Lightweight Packaging Design: Request factories to recommend “degradable + thin-walled” packaging (e.g., PETG material replacing traditional glass), which reduces single-bottle packaging cost by 8%-12% and complies with EU ESG packaging requirements;​
  1. Production Cycle Optimization: Avoid placing orders in Q4 (Double 11, Christmas peak season) and choose to cooperate in Q2. Factories offer 5%-8% lower quotations when production capacity is sufficient, and sample development cycles are shortened to 5 days;​
  1. Testing Cost Sharing: For orders < 1,000 units, negotiate with factories for “shared testing reports among multiple brands in the same batch”. The testing fee per product decreases from 800 yuan to 300 yuan (ensure the testing institution is CNAS-accredited ).​

(II) Professional Support: Implementation Steps for 2025 New Compliance Requirements​

  1. Raw Material Compliance:​
  • Request factories to provide “raw material safety information submission certificates” (raw materials not submitted cannot be used in production starting from 2025), with key verification of “new raw material” (e.g., hydroxydecyl ubiquinone) usage authorization;​
  • Imported raw materials require additional “Chinese label registration certificates” to avoid notifications from drug regulatory authorities due to incomplete label information (12% of factories were penalized for this issue in 2025).​
  1. Production Compliance:​
  • Verify the qualification certificate of the factory’s “Quality Safety Principal” (must have a bachelor’s degree or above in cosmetic-related majors + 5+ years of work experience);​
  • Request “real-time cleanliness monitoring records” of production workshops (Class 100,000 clean workshops require hourly testing, with suspended particle count ≤ 352,000 particles/m³).​

(III) Authority Endorsement: 3 Verifiable Proofs of Factory Capability​

  1. Industry Certifications: In addition to ISO 22716 and GMPC, prioritize factories certified under China’s “Cosmetic Good Manufacturing Practice (GMP)” . Only 30% of top-tier factories obtained this certification in 2025;​
  1. Client Cases: Request factories to provide “cooperation certificates with well-known brands in the same category” (e.g., copies of OEM contracts with major domestic skincare brands), which can be cross-verified via brand official websites or e-commerce product pages;​
  1. Testing Reports: Request “finished product sampling reports” from the past 3 months, which must include “prohibited substance screening” (e.g., glucocorticoids, antibiotics). Testing institutions must be listed in the “Cosmetic Testing Institution Directory” of the National Medical Products Administration.​

(IV) Trust Building: 6 Must-Include Safeguard Clauses in Contracts (Dispute Prevention)​

  1. Compliance Compensation: If products are removed from shelves due to factory compliance issues (e.g., unregistered raw materials), the factory shall bear all losses (including goods value + fines + brand reputation compensation. It is recommended to stipulate compensation ≥ 2 times the order amount);​
  1. Cost Transparency: Clarify raw material brands, specifications, and procurement prices (e.g., “using Bloomage Biotechnology 4D Hyaluronic Acid at 800 yuan/kg”) and prohibit factories from replacing with low-cost raw materials without authorization;​
  1. Sample Retention Liability: Factories shall retain 3 samples per batch (each ≥ 100g/ml) for ≥ 3 years. Brands may inspect sample status at any time;​
  1. After-Sales Response: Solutions for quality issues must be provided within 24 hours, and re-inspection arranged within 48 hours, with re-inspection fees borne by the factory;​
  1. Production Capacity Guarantee: Stipulate “peak season capacity reservation” (e.g., factories reserve ≥ 50% of production lines for the brand 2 months before Double 11);​
  1. Enhanced Confidentiality: In addition to formula confidentiality, additionally stipulate “customer information confidentiality” to prohibit factories from disclosing brand sales data and pricing strategies to competitors.​

III. Customized Cooperation Plans for Brands of Different Scales (Precise Demand Matching)​

(I) Startup Brands (Monthly Orders < 5,000 Units)​

  • Factory Selection: Prioritize medium-sized factories in Huadu (Guangzhou) and Nanhai (Foshan). These factories have MOQs as low as 300 units and provide one-stop services including “formula optimization + packaging design” with low cooperation thresholds;​
  • Cost Control: Choose “semi-finished product OEM” initially (factories produce creams/liquids, brands purchase packaging independently), which costs 15% less than finished product OEM;​
  • Compliance Focus: Focus on verifying factories’ “registration agency capabilities” to ensure product completion of domestic non-special cosmetic registration within 45 days .​

(II) Growing Brands (Monthly Orders 5,000-20,000 Units)​

  • Factory Selection: Cooperate with factories in Hangzhou and Suzhou, which have rich experience in OEM of “functional products” (e.g., anti-aging, whitening) and access to “clinical efficacy testing” resources;​
  • Cooperation Model: Sign “quarterly framework agreements” specifying total quarterly orders. Factories offer 3%-5% price discounts while ensuring stable production capacity;​
  • Compliance Focus: Require factories to participate in “cosmetic adverse reaction monitoring” and submit monthly adverse reaction reports to reduce market risks.​

(III) Mature/Cross-Border Brands (Monthly Orders > 20,000 Units)​

  • Factory Selection: Prioritize top-tier factories such as Cosmax (China) and Intercos (Shanghai), which have “multi-category simultaneous production” capabilities (e.g., skincare, makeup, perfume) and cross-border compliance teams;​
  • Cost Reduction Techniques: Sign “annual strategic cooperation agreements” specifying annual procurement volume to obtain raw material group purchase prices + free formula upgrading services;​
  • Compliance Focus: For target markets (e.g., EU, ASEAN), request factories to provide “local compliance certifications” (e.g., EU CPSR reports, ASEAN cosmetic registration certificates) to ensure smooth customs clearance.​

IV. Risk Preparedness Toolkit (Directly Reusable)​

  1. Factory Compliance Checklist: Includes 12 mandatory verification items such as “production license, raw material registration certificate, quality safety principal qualification” for step-by-step verification;​
  1. Cost Calculation Template: Automatically calculates per-product costs by inputting order quantity, raw material specifications, and packaging type to avoid overquoting by factories;​
  1. Cross-Border Compliance Guide: Categorizes prohibited ingredients, labeling requirements, and customs clearance procedures by region (EU, ASEAN, North America) for direct reference by factories.

发表回复

您的邮箱地址不会被公开。 必填项已用 * 标注