An R&D area covering laboratory-scale synthesis, process development, verification, and scale-up studies for pharmaceutical raw materials and special-purpose chemical compounds. High-purity pharmaceutical compounds compliant with international standards are synthesized.
Synthesis, purification, and analysis of active pharmaceutical ingredients (APIs) are supported by GMP-standard production process development and scale-up studies.
Determining optimum reaction conditions for the target molecule and optimizing yield and selectivity.
Obtaining high-purity products through methods such as crystallization, distillation, and column chromatography.
Structural characterization and purity determination using HPLC, GC, NMR, FTIR, and mass spectrometry.
Transition from laboratory scale to pilot production, process validation, and reproducibility studies.
A sterile gauze compress system that combines hemostatic support for bleeding control with hygiene support on the wound surface.
Learn MoreHemostatic formulations developed for rapid clotting and bleeding control, in powder, granule, impregnated gauze, and spray forms.
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