API Impurities
KASAM Therapeutics specializes in the production and supply of pharmaceutical impurities essential for pharmaceutical companies to assess the quality, stability, and biological safety of their products. Even trace amounts of impurities can impact the efficacy of an Active Pharmaceutical Ingredient (API) and may sometimes cause unwanted side effects, making it crucial to monitor and control their levels. The guidelines and limits for various impurities are specified in the respective pharmacopeia monographs.
All our impurities and standards come with a Certificate of Analysis (CoA) and comprehensive characterization data, including 1H-NMR, mass spectrometry, and HPLC purity.
At KASAM Therapeutics, we synthesize impurities using reliable scientific methods, including organic synthesis, enrichment and isolation by chromatography, and degradation and isolation processes. The pharmaceutical (API/drug) impurities we produce are invaluable for generating and evaluating data that establish the quality, stability, and biological safety of pharmaceutical products.
