· Exclusive synthesis services forpharmaceutical intermediates and API
· Process research and development ofbest synthetic pathways, process parameters research
· Processoptimization, scale-up and validation
· Development and validation ofanalytical methods
· Supply of intermediates/activepharmaceutical ingredients for preclinical trials (pre-IND), different clinicalstages and batch production after commercialization
· Productioncapacity in the GMP workshop from kilograms to tens of tons
· Stability test that conforms to ICHstandards
· Drugapplication (CMC/DMF) support
· Complete GMP control system
· Never compete with customers forterminal markets
· Neverinfringe on customers’ intellectual properties