GLP Pharma Standards relies on their expert research team with strong scientific and academic backgrounds and a rich discovery experience. GLP Pharma Standards is ever eager to take up even the most challenging synthesis processes.
GLP Pharma Standsrds scientists are experts at performing complex, multi-step syntheses and developing custom molecules (CRO) as per customer’s requirements.
The synthesis laboratories at GLP Pharma Standards have a broad range of capabilities that can be applied in fulfilling customers’ synthetic chemistry needs, especially the custom syntheses of low volume, high value products for pharmaceutical impurities and metabolites.
API Impurities and Metabolites
GLP Pharma Standards is specialized in providing high quality API Impurities, Drug Working Standards, Reference Standards, Drug Metabolites, Genotoxic Impurities and Stable Isotope Labelled compounds as per the clients requirements at reasonable prices.
• Custom products can be synthesized using methods designed by the custom synthesis team • Potential for transfer to large scale manufacturing facilities and GMP facilities as well.
Isolation, Identification and Characterization of Unknown Impurities
• Isolation and purification for both existing compounds and new Chemical/Biological Entities. • Stress degradation to understand degradation chemistry • Structure Elucidation by Mass, HNMR, C13, IR etc..
Complex Chiral Compounds
GLP Pharma have broad range of capabilities in developing of complex, multi-step synthesis molecules and we have expert scientist teams to solve difficult chemistry problems.