In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a C15H13N3O4S Drug Master File in Korea (C15H13N3O4S KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of C15H13N3O4S. The MFDS reviews the C15H13N3O4S KDMF as part of the drug registration process and uses the information provided in the C15H13N3O4S KDMF to evaluate the safety and efficacy of the drug.
After submitting a C15H13N3O4S KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their C15H13N3O4S API can apply through the Korea Drug Master File (KDMF).
click here to find a list of C15H13N3O4S suppliers with KDMF on PharmaCompass.