New Drug(NCE) CDMO Service

Based on the strict quality control and high purity API manufacturing technologies, Kyongbo is routinely inspected by Korean and overseas regulatory authorities from Japan, U.S, Europe and etc and is cGMP certified.

Since Kyongbo Pharmaceutical’s establishment in 1987 it has been concentrating its business on the API manufacturing.

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.