Comprehensive solutions for quality control of medicines and pharmaceutical industries, ensuring compliance with international standards.
Certified Reference Materials Development
- Manufacturing of pharmacopoeia-grade certified reference standards
- Custom development of API and related substance reference materials
- Full method validation according to current GMP and ICH Q2(R1)
Pharmaceutical Analytical Services
- Chromatographic separations (HPLC, GC, TLC)
- Spectroscopic characterization (UV-Vis, FTIR, refractometry, polarimetry)
- Dissolution profile comparison and bioanalytical method development
- Comprehensive pharmacopoeial compliance testing
API Development with Technology Transfer
- Full-cycle synthesis of active pharmaceutical ingredients (APIs)
- Process optimization of manufacturing technologies
- Turnkey production solutions delivery (technology transfer)
Supply of Intermediates
- High-quality intermediate compounds for API synthesis
- Compliance with strict purity and stability standards
Impurity Standards Supply
- Certified and fully characterized impurity standards for analytical method validation
Chromatography Column Solutions
- Extensive portfolio of HPLC/GC stationary phases
- Application-specific column selection
- Method development and optimization support