Service Model

Choose the right collaboration model for your stage.

Four approaches tailored to four customer stages: those with existing formulations, clients needing full development from scratch, teams validating the market, or businesses preparing to go global.

Minimum Order Quantity for Sampling
500 pcs
Category coverage
Skincare / Personal Care / Makeup / Oral Care
Compliant Market
EU / US / Southeast Asia
Real footage of automated filling production line
Real footage of automated filling production line
01

OEM manufacturing

Ideal for brands that have completed formula and packaging development. We organize filling, packaging, and outgoing inspection based on the customer-approved formulation and packaging materials. Process records are archived by batch for easy traceability and reordering.

Suitable for:Brands and distributors with established formulas and packaging systems

Services Offered

  • Incoming Inspection: Verify and sample-check raw materials and packaging upon arrival by batch.
  • Filling and Packaging: Execute according to the confirmed process parameters and packaging method.
  • Process logs: Trace key steps and trace back abnormal batches.
  • Outgoing Inspection: Verify appearance, net content, and packaging integrity per batch.

Delivery Process

  1. 1Requirements and Materials Confirmation
  2. 2Incoming Quality Control
  3. 3Filling and packaging
  4. 4Outgoing Inspection
  5. 5Delivery and Archiving
Real photos of the packaging design studio
02

ODM Full-Service Development

Start with a product concept. Our formulation team handles recipe design and prototyping, coordinates packaging selection and visual execution, and completes all regulatory filing documentation before mass production—reducing communication overhead from managing multiple vendors.

Suitable for:Need a brand and content e-commerce team to launch new products from 0 to 1.

Service Offerings

  • Concept Overview: Define Category, Positioning, Cost Range, and Use Cases
  • Formula R&D: Adjust existing formulas or develop targeted new ones
  • Packaging & Visuals: Provide selection recommendations and coordinate sample confirmation.
  • Registration Filing: Submit formulation, testing, and labeling documents simultaneously.

Delivery Process

  1. 1Concept Alignment
  2. 2Formula Design
  3. 3Sample Confirmation
  4. 4Packaging and Filing
  5. 5Pilot and Mass Production
Small-batch sample development, real photos
03

Small-batch prototyping

Ideal for brands in the validation phase. Conduct real-world product and packaging trials with low MOQs, gather market feedback, and decide on scaling up to avoid overstocking.

Suitable for:First product of a new brand; test new category for an established brand

Service Offerings

  • Flexible MOQ: Order as few as 500 units to minimize pilot production costs.
  • Pilot Run: Conducted on the mass production line with identical processes.
  • Feedback loop: Adjust formulas or packaging based on trial feedback.
  • Scale-up transition: Proceed according to mass production schedule after validation.

Delivery Process

  1. 1Requirement Confirmation
  2. 2Formula prototyping
  3. 3Sample confirmation
  4. 4Pilot Production
  5. 5Feedback and Scaling
Real photos of quality control inspections
04

Cross-border Compliance Services

Compliance documentation for international products spans formulas, testing reports, labels, and responsible parties. We organize the required document checklist by target market, assist in preparing and submitting materials, and minimize delays caused by incomplete submissions.

Suitable for:Brands and cross-border channels targeting the EU, US, and Southeast Asian markets

Services

  • EU CPSR: Compile Basic Documentation for Formula and Safety Assessment
  • U.S. FDA: Prepare product and facility information in cooperation
  • ASEAN Filing: Prepare submission documents per target country requirements
  • Label Compliance: Verify ingredient labeling and required warnings

Delivery Process

  1. 1Market Confirmed
  2. 2Document Checklist
  3. 3Diagnostics pairing
  4. 4Submit File
  5. 5Archive and Reuse
How to choose

OEM or ODM

The difference isn't just about who provides the formula—it also lies in packaging, regulatory filing, and communication costs.

Minimum Order Quantity for Sample

500Minimum order quantity

Ideal for new brands validating the market and mature brands testing new product categories. Prototyping and small-batch pilot runs are completed on full-scale production lines, ensuring processes match mass production standards.

Comparison ItemsOEM manufacturingODM Full-Service Development
Recipe SourceCustomer provides formulation and process requirementsFactories develop or design on demand based on the formula library.
PackagingCustomer-provided packaging materials are inspected upon arrival at the facility before filling.Assist in component selection and prototype validation to support visual implementation.
FilingFollow the client's provided materials.Process formula, testing, and labeling documentation in parallel.
Suitable PhaseBrand owners with a mature product ecosystemBrand for launching new products from 0 to 1

Both methods can be used to prepare cross-border compliance documentation, depending on the target market.

Frequently Asked Questions

Common Questions Before We Start Working Together

What is the minimum order quantity?

Minimum order quantity for sampling and small-batch trial production is 500 units. The MOQ for mass production will be confirmed based on product category, packaging materials, and manufacturing processes.

How long does sampling take?

Sample scheduling depends on formula complexity and packaging material availability. Once requirements and documents are confirmed, we will provide the corresponding schedule and milestones.

Can packaging be handled together?

Yes. ODM full-service development includes packaging material selection recommendations and sample approval. In OEM mode, the client provides the packaging materials, and we proceed with filling after inspecting the incoming materials.

Who is responsible for filing the declaration?

We assist with both domestic filing and cross-border compliance. We organize formula, testing, and labeling documentation for submission, while the declaring entity confirms all requirements per regulations.

Can I visit your factory?

Factory tours are available upon request. Visits will follow cleanroom safety protocols; please confirm your appointment in advance.

Online Inquiry

Not sure which method to choose?

Share your product concept, target positioning, and estimated volume. We'll provide partnership recommendations.

Business hours 09:00 - 18:00: Business consultants get priority response