Our system focuses on standardized manufacturing environments, 12-step inspection, raw material sourcing, batch traceability, export documentation, and transparent certification progress.
Quality Audit Roadmap
We are currently progressing through third-party quality audit preparation. The facility operates under structured internal frameworks while third-party certificates are finalized.
Standardized Manufacturing Environment
GMP-based hygiene, personnel, and process controls are used for veterinary and functional pet product production.
Following International Export Guidelines
Export documents, formula details, and batch records can be prepared according to buyer market requirements.
Export Documentation
Commercial invoice, packing list, COA, product specification, and other shipment documents are prepared by order type.
Batch Precision
Full digital batch records available for every run, including precise raw material sourcing and testing logs.
Scientific Validation
In-house QC can be combined with optional third-party laboratory testing according to the target market and buyer requirements.
Every ingredient undergoes identity and purity verification. We screen for heavy metals, pesticides, and microbiological safety before acceptance.
Fully automated monitoring of critical parameters: humidity, temperature, and extrusion precision to maintain batch consistency.
Finished batches are subjected to accelerated stability tests to ensure shelf-life stability and flavor integrity in diverse climates.
100% batch testing for nutritional markers and active ingredients. Full documentation (COA) is generated for every global shipment.
Batch samples are retained in our climate-controlled library for 2 years, allowing for post-market traceability and quality verification.
