Analytical Research and Development Department
analytical method development and validation and regulatory compliance to ensure all analytical work follows good manufucturing practices (GMP)requriments project tittle :development and validation of HPLC method for quantification of active pharmaceutical ingredient (API) in a new drug formulation The goal of this project is to develop and validate a robust high performance liquid chromatography ( HPLC) method for the accurate quantifocation of an active pharmaceutical ingredient (API) in a newly developed oral solid dosage form(tablet)