We follow rigorous international standards to ensure every product complies with safety and regulatory requirements.

Every Xidafeng formulation undergoes 143+ quality checkpoints aligned with FDA 21 CFR, EU REACH Annex XVII, and ISO 17025 protocols. Our blockchain-tracked production process ensures raw material purity from GMP-certified facilities, with HPLC/GC-MS analysis verifying 99.9% ingredient traceability. Third-party audits by SGS and NSF International certify compliance with HACCP, Kosher, and Halal standards across nutraceutical, cosmetic, and homecare product lines.

Multilingual regulatory specialists monitor 50+ international chemical inventories (TSCA, IECSC, K-REACH), delivering country-specific SDS documentation and EFSA/ECHA dossier preparation. Through AI-powered regulatory gap analysis and annual 12,000+ stability tests under ICH Q1A conditions, we achieve 100% customs clearance success in target markets while pioneering OECD 403-certified alternatives to animal testing.

Our Shenzhen-based Quality 4.0 Lab deploys machine learning models trained on 850,000+ historical test records to predict formulation deviations with 94.3% accuracy. We pioneered CRISPR-based rapid microbial detection systems (patent pending CN202310000123.5) that slash pathogen screening time from 72hrs to 45min while exceeding ISO 16140-3 validation criteria. With 18% annual R&D reinvestment and 37 patent-pending green chemistry breakthroughs – including enzyme-catalyzed solvent-free emulsifiers – Xidafeng redefines quality as dynamic value creation, where ISO 9001 compliance converges with UN SDG-driven disruptive innovation.