Provides high-quality intermediates essential for active pharmaceutical ingredient (API) development. Supplies process-related, degradation, and potential impurities for regulatory submissions. Ensures compliance with global pharmacopeial standards and GMP practices.
Impurities, degradants and metabolites of active pharmaceutical and excipients. Isolation, purification and characterisation of high purity compounds and complex molecules. Milligram to multigram scale Analysis to your requirements including NMR, LCMS, GCMS, HPLC, IR and water content. Isolation & Structure Elucidation Of Unknown Impurities Pharmaceutical Reference Standards Contract Research Services Development of new synthetic routes Delivering custom synthesis at off the shelf pricing Process research, development and optimization Cost-effective and high efficiency
Provides high-quality intermediates essential for active pharmaceutical ingredient (API) development. Supplies process-related, degradation, and potential impurities for regulatory submissions. Ensures compliance with global pharmacopeial standards and GMP practices.