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