Quality, Certifications, and Factory Audit Readiness

The quality page is for procurement, R&D, and sourcing teams that need factory proof before sharing formulas or placing orders. It summarizes quality references, GMPC and ISO 22716 references, BFS factory capability, confidentiality workflow, QC checkpoints, and global buyer support.

Documents qualified buyers can ask to review

• GMPC and ISO 22716 quality-system references
• Factory capability pack with two-site manufacturing overview and 21 BFS lines
• Equipment records, cleanroom evidence, and QC checkpoint summary
• NDA process before proprietary formula recipe transfer
• Batch documentation, COA path, and export documentation review by project

Confidential formula workflow

Buyers should not paste full proprietary formulas into a public form. Start with product type, formula status, target fill volume, active sensitivity, launch market, MOQ range, and timeline. Full formula recipe transfer should happen after NDA alignment.

Anonymized buyer patterns

• Clinic / spa sample serum pilot from 5,000-unit high-potential review into 10,000-unit MOQ planning
• NDA formula transfer route for proprietary skincare contract filling
• Trial kit and GWP ampoule route for single-dose sampling programs

Next step

Request a quality documentation review or open the factory capability page.