Quality, accuracy, safety — verified on every batch
Each batch we supply passes staged quality assurance and quality control before release, helping guarantee the safety of the finished product for end users.
Our approach
Quality is designed in, then tested for
Our production facilities are designed in strict compliance with GMP standards, and we invest continuously in the analytical capability of our QC laboratory so that test results are accurate and objective.
- Staged quality assurance and quality control on every batch
- GMP-compliant facility design at both production sites
- Dedicated QC laboratory with modern branded analytical instruments
- Emphasis on innovation and environment-friendly technologies
Capability
QC laboratory equipment
The laboratory is equipped for the full analytical scope required to test APIs and intermediates accurately and objectively.
- HPLC / LC-MS
- GC (gas chromatography)
- ICS (ion chromatography)
- IS spectroscopy
- UV spectrophotometry
- Water determination
- Analytical balances
- Particle size analyzer
- Drug stability test chambers
Facilities
Inside the QC laboratory
Documentation
Working documentation for your filings
Specifications, analytical test methods, stability data, impurity profiles and reference standards are part of the API technology packages we prepare for customers — see our technology transfer service for the full scope.
Technology transfer & documentationManufacturing
Where our products are made
Production takes place at facilities in Anhui and Shanxi provinces, designed in strict compliance with GMP standards.
Manufacturing capabilitiesStart an inquiry
Ready to discuss your requirements?
Send us the product name or CAS number, the quantity you need, and your destination market — our team will respond with specifications, availability and lead times.