In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a C18H23NO.C6H8O7 Drug Master File in Korea (C18H23NO.C6H8O7 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of C18H23NO.C6H8O7. The MFDS reviews the C18H23NO.C6H8O7 KDMF as part of the drug registration process and uses the information provided in the C18H23NO.C6H8O7 KDMF to evaluate the safety and efficacy of the drug.
After submitting a C18H23NO.C6H8O7 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 C18H23NO.C6H8O7 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of C18H23NO.C6H8O7 suppliers with KDMF on PharmaCompass.