In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a C12H17NO2.C2H7NO Drug Master File in Korea (C12H17NO2.C2H7NO KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of C12H17NO2.C2H7NO. The MFDS reviews the C12H17NO2.C2H7NO KDMF as part of the drug registration process and uses the information provided in the C12H17NO2.C2H7NO KDMF to evaluate the safety and efficacy of the drug.
After submitting a C12H17NO2.C2H7NO 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 C12H17NO2.C2H7NO API can apply through the Korea Drug Master File (KDMF).
click here to find a list of C12H17NO2.C2H7NO suppliers with KDMF on PharmaCompass.