Kyongbo started its CDMO business for CKD Pharm and Crystalgenomics’ NCEs (New Chemical Entities) and
starting from these experiences, we have now the specialized technology in the new drug studies from
the early stage to process development & improvement up to commercialization.
Kyongbo has independently separated facilities capable of manufacturing general APIs, cephalosporin and
carbapenem antibiotics, cytotoxic anti-cancer APIs and high potency APIs. The quality control is also
separated.
Recently, Kyongbo plays a role as a partner to develop domestic and overseas NCE APIs and through know-
how based on the long experiences from R&D, production and quality department, Kyongbo provides the
problem solving skills and customer specific CMC relevant documentation required by the government
regulatory agencies.
Kyongbo Pharm will continue to contribute to the developing of new drugs both domestic and overseas
through working timely and efficiently as a new drug developing partner.