Quality Control unit at GenPep can perform the comprehensive assessment of structural integrity and purity of the peptide. We are committed to develop a robust analytical method and subsequently validation with appropriate documentations to meet the GMP compliances. Our analytical expertise can perform the key raw material and finished product analysis as per the guideline published by regulatory bodies, such as ICH (International Conference on Harmonization), FDA (Food and Drug Administration) or EMEA (European Agency for the Evaluation of Medicinal Products)