● Physical chemical evaluation of test articles

● Formulation development and selection - injectable, oral, topical and inhalation

●Analytical method development and validation

● Dosage form manufacturing process development, optimization and scale-up

● Manufacture of preclinical and clinical supplies as well as NDA batches

● Stability programs - IND, Phase I, II and III, as well as NDA batches

● CMC document preparation - IND and NDA