Guangzhou, Chinaaxdwlab@gmail.com

R&D & Manufacturing · Guangzhou, China

Cosmetic Formulation
& Manufacturing

Discuss development, sample validation and production scheduling around your product positioning, desired product characteristics and packaging requirements.

Laboratory weighing and sample preparation worksite photo
Laboratory weighing and sample preparation · View original photo

Formulation Development Around Your Product Goals

Product Positioning

Usage scenarios, target markets and reference samples.

Formula Direction

Discuss ingredient selection, texture and scent.

Sample Iteration

Evaluate skin feel, appearance and user experience.

Formula & Packaging Compatibility

Evaluate compatibility with packaging components and processes.

From Sample Performance to a Validation Plan

Stability Observation

Discuss observation conditions and record requirements.

Packaging Compatibility

Plan compatibility evaluations for the formula and packaging components.

Physical & Chemical Parameters

Determine applicable parameters and methods for the product.

Microbiological Testing

Discuss applicable tests and documentation requirements.

Test scope, methods and documentation are confirmed for each product and project. These items do not mean that all products have passed testing.

Connect Development with the Manufacturing Process

  1. Raw Material & Packaging Confirmation

  2. Compounding & Process Control

  3. Bulk Product Inspection

  4. Filling & Sealing

  5. Label & Packaging Checks

  6. Finished Product Inspection & Release

Among the local materials reviewed, no worksite photo clearly showing the filling stage has yet been confirmed.

Quality Control at Key Stages

Incoming Material Confirmation

Check raw material and packaging specifications against project requirements.

Process Checks

Discuss inspection arrangements for compounding, filling and packaging.

Finished Product Checks

Check finished goods against approved samples and project agreements.

Batches & Changes

Coordinate batch records and version change requirements.

Review Relevant Documentation for Your Project

Company & Manufacturing Qualifications

Review relevant documentation at the appropriate stage of cooperation.

Product Testing Documentation

Discuss documentation for the product and applicable tests.

Project & Batch Records

Coordinate development and manufacturing records within the project scope.

The certificate holder, scope and validity period are subject to the original image and project-specific verification. Document categories do not mean that every product has all documents; availability depends on existing records and project scope.

See the Worksite and Continue the Discussion

Discuss a video or on-site visit, with the schedule and accessible areas confirmed in advance.

Intended Sales Markets (Select All That Apply)

Select multiple markets if needed. Add any country or region not listed below.

You do not need to provide complete formulas or confidential documents for an initial inquiry.

Your requirements will be saved for our team to review.

ISO 22716:2007 Certificate Documentation

Full Original ISO 22716:2007 Certificate, with Original Holder and Validity Period PreservedOpen Full-Size Image